Erratum: An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 (The American Journal of Human Genetics (2023) 110(1) (105–119), (S0002929722005067), (10.1016/j.ajhg.2022.11.015))

Haloom Rafehi; Justin Read; David J. Szmulewicz; Kayli C. Davies; Penny Snell; Liam G. Fearnley; Liam Scott; Mirja Thomsen; Greta Gillies; Kate Pope; Mark F. Bennett; Jacob E. Munro; Kathie J. Ngo; Luke Chen; Mathew J. Wallis; Ernest G. Butler; Kishore R. Kumar; Kathy HC Wu; Susan E. Tomlinson; Stephen Tisch; Abhishek Malhotra; Matthew Lee-Archer; Egor Dolzhenko; Michael A. Eberle; Leslie J. Roberts; Brent L. Fogel; Norbert Brüggemann; Katja Lohmann; Martin B. Delatycki; Melanie Bahlo; Paul J. Lockhart

doi:10.1016/j.ajhg.2023.05.005

Erratum: An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 (The American Journal of Human Genetics (2023) 110(1) (105–119), (S0002929722005067), (10.1016/j.ajhg.2022.11.015))

Haloom Rafehi, Justin Read, David J. Szmulewicz, Kayli C. Davies, Penny Snell, Liam G. Fearnley, Liam Scott, Mirja Thomsen, Greta Gillies, Kate Pope, Mark F. Bennett, Jacob E. Munro, Kathie J. Ngo, Luke Chen, Mathew J. Wallis, Ernest G. Butler, Kishore R. Kumar, Kathy HC Wu, Susan E. Tomlinson, Stephen TischAbhishek Malhotra, Matthew Lee-Archer, Egor Dolzhenko, Michael A. Eberle, Leslie J. Roberts, Brent L. Fogel, Norbert Brüggemann, Katja Lohmann, Martin B. Delatycki, Melanie Bahlo^*, Paul J. Lockhart^*

^*Korrespondierende/r Autor/-in für diese Arbeit

33 Zitate (Scopus)

Abstract

(The American Journal of Human Genetics 110, 105–119; January 5, 2023) After publication of this article, the autosomal-dominant adult-onset ataxia the authors preliminarily called SCA50 was officially named SCA27B by OMIM. The title and text have now been updated to reflect this name change.

Originalsprache	Englisch
Zeitschrift	American Journal of Human Genetics
Jahrgang	110
Ausgabenummer	6
Seiten (von - bis)	1018
Seitenumfang	1
ISSN	0002-9297
DOIs	https://doi.org/10.1016/j.ajhg.2023.05.005
Publikationsstatus	Veröffentlicht - 01.06.2023

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

SDG 3 – Gesundheit und Wohlergehen
SDG 10 – Weniger Ungleichheiten

Strategische Forschungsbereiche und Zentren

Querschnittsbereich: Medizinische Genetik

Dokumente

10.1016/j.ajhg.2023.05.005

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Rafehi, H., Read, J., Szmulewicz, D. J., Davies, K. C., Snell, P., Fearnley, L. G., Scott, L., Thomsen, M., Gillies, G., Pope, K., Bennett, M. F., Munro, J. E., Ngo, K. J., Chen, L., Wallis, M. J., Butler, E. G., Kumar, K. R., Wu, K. HC., Tomlinson, S. E., ... Lockhart, P. J. (2023). Erratum: An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 (The American Journal of Human Genetics (2023) 110(1) (105–119), (S0002929722005067), (10.1016/j.ajhg.2022.11.015)). American Journal of Human Genetics, 110(6), 1018. https://doi.org/10.1016/j.ajhg.2023.05.005

Rafehi, Haloom ; Read, Justin ; Szmulewicz, David J. et al. / Erratum : An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 (The American Journal of Human Genetics (2023) 110(1) (105–119), (S0002929722005067), (10.1016/j.ajhg.2022.11.015)). in: American Journal of Human Genetics. 2023 ; Jahrgang 110, Nr. 6. S. 1018.

@article{f29a1d61d48c4442afcc1146822ee919,

title = "Erratum: An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 (The American Journal of Human Genetics (2023) 110(1) (105–119), (S0002929722005067), (10.1016/j.ajhg.2022.11.015))",

abstract = "(The American Journal of Human Genetics 110, 105–119; January 5, 2023) After publication of this article, the autosomal-dominant adult-onset ataxia the authors preliminarily called SCA50 was officially named SCA27B by OMIM. The title and text have now been updated to reflect this name change.",

author = "Haloom Rafehi and Justin Read and Szmulewicz, \{David J.\} and Davies, \{Kayli C.\} and Penny Snell and Fearnley, \{Liam G.\} and Liam Scott and Mirja Thomsen and Greta Gillies and Kate Pope and Bennett, \{Mark F.\} and Munro, \{Jacob E.\} and Ngo, \{Kathie J.\} and Luke Chen and Wallis, \{Mathew J.\} and Butler, \{Ernest G.\} and Kumar, \{Kishore R.\} and Wu, \{Kathy HC\} and Tomlinson, \{Susan E.\} and Stephen Tisch and Abhishek Malhotra and Matthew Lee-Archer and Egor Dolzhenko and Eberle, \{Michael A.\} and Roberts, \{Leslie J.\} and Fogel, \{Brent L.\} and Norbert Br{\"u}ggemann and Katja Lohmann and Delatycki, \{Martin B.\} and Melanie Bahlo and Lockhart, \{Paul J.\}",

note = "Publisher Copyright: {\textcopyright} 2023",

year = "2023",

month = jun,

day = "1",

doi = "10.1016/j.ajhg.2023.05.005",

language = "English",

volume = "110",

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Rafehi, H, Read, J, Szmulewicz, DJ, Davies, KC, Snell, P, Fearnley, LG, Scott, L, Thomsen, M, Gillies, G, Pope, K, Bennett, MF, Munro, JE, Ngo, KJ, Chen, L, Wallis, MJ, Butler, EG, Kumar, KR, Wu, KHC, Tomlinson, SE, Tisch, S, Malhotra, A, Lee-Archer, M, Dolzhenko, E, Eberle, MA, Roberts, LJ, Fogel, BL, Brüggemann, N , Lohmann, K, Delatycki, MB, Bahlo, M & Lockhart, PJ 2023, 'Erratum: An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 (The American Journal of Human Genetics (2023) 110(1) (105–119), (S0002929722005067), (10.1016/j.ajhg.2022.11.015))', American Journal of Human Genetics, Jg. 110, Nr. 6, S. 1018. https://doi.org/10.1016/j.ajhg.2023.05.005

Erratum: An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 (The American Journal of Human Genetics (2023) 110(1) (105–119), (S0002929722005067), (10.1016/j.ajhg.2022.11.015)). / Rafehi, Haloom; Read, Justin; Szmulewicz, David J. et al.
in: American Journal of Human Genetics, Jahrgang 110, Nr. 6, 01.06.2023, S. 1018.

Publikation: Beiträge in Fachzeitschriften › Kommentare/Debatten

TY - JOUR

T1 - Erratum

T2 - An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 (The American Journal of Human Genetics (2023) 110(1) (105–119), (S0002929722005067), (10.1016/j.ajhg.2022.11.015))

AU - Rafehi, Haloom

AU - Read, Justin

AU - Szmulewicz, David J.

AU - Davies, Kayli C.

AU - Snell, Penny

AU - Fearnley, Liam G.

AU - Scott, Liam

AU - Thomsen, Mirja

AU - Gillies, Greta

AU - Pope, Kate

AU - Bennett, Mark F.

AU - Munro, Jacob E.

AU - Ngo, Kathie J.

AU - Chen, Luke

AU - Wallis, Mathew J.

AU - Butler, Ernest G.

AU - Kumar, Kishore R.

AU - Wu, Kathy HC

AU - Tomlinson, Susan E.

AU - Tisch, Stephen

AU - Malhotra, Abhishek

AU - Lee-Archer, Matthew

AU - Dolzhenko, Egor

AU - Eberle, Michael A.

AU - Roberts, Leslie J.

AU - Fogel, Brent L.

AU - Brüggemann, Norbert

AU - Lohmann, Katja

AU - Delatycki, Martin B.

AU - Bahlo, Melanie

AU - Lockhart, Paul J.

PY - 2023/6/1

Y1 - 2023/6/1

N2 - (The American Journal of Human Genetics 110, 105–119; January 5, 2023) After publication of this article, the autosomal-dominant adult-onset ataxia the authors preliminarily called SCA50 was officially named SCA27B by OMIM. The title and text have now been updated to reflect this name change.

AB - (The American Journal of Human Genetics 110, 105–119; January 5, 2023) After publication of this article, the autosomal-dominant adult-onset ataxia the authors preliminarily called SCA50 was officially named SCA27B by OMIM. The title and text have now been updated to reflect this name change.

UR - https://www.scopus.com/pages/publications/85160365142

U2 - 10.1016/j.ajhg.2023.05.005

DO - 10.1016/j.ajhg.2023.05.005

M3 - Comments/Debates

C2 - 37267898

AN - SCOPUS:85160365142

SN - 0002-9297

VL - 110

SP - 1018

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 6

ER -

Rafehi H, Read J, Szmulewicz DJ, Davies KC, Snell P, Fearnley LG et al. Erratum: An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 (The American Journal of Human Genetics (2023) 110(1) (105–119), (S0002929722005067), (10.1016/j.ajhg.2022.11.015)). American Journal of Human Genetics. 2023 Jun 1;110(6):1018. doi: 10.1016/j.ajhg.2023.05.005