Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209)

Diana Braunholz; Melanie Hullings; María Concepcion Gil-Rodríguez; Christopher T. Fincher; Mark B. Mallozzi; Elizabeth Loy; Melanie Albrecht; Maninder Kaur; Janusz Limon; Abhinav Rampuria; Dinah Clark; Antonie Kline; Andreas Dalski; Juliane Eckhold; Andreas Tzschach; Raoul Hennekam; Gabriele Gillessen-Kaesbach; Jolanta Wierzba; Ian D. Krantz; Matthew A. Deardorff; Frank J. Kaiser

doi:10.1038/ejhg.2011.209

Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209)

Diana Braunholz^*, Melanie Hullings, María Concepcion Gil-Rodríguez, Christopher T. Fincher, Mark B. Mallozzi, Elizabeth Loy, Melanie Albrecht, Maninder Kaur, Janusz Limon, Abhinav Rampuria, Dinah Clark, Antonie Kline, Andreas Dalski, Juliane Eckhold, Andreas Tzschach, Raoul Hennekam, Gabriele Gillessen-Kaesbach, Jolanta Wierzba, Ian D. Krantz, Matthew A. DeardorffFrank J. Kaiser

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

Institut für Humangenetik

Abstract

Since the publication of this article, the authors noted that NIPBL was mistyped in several places. This has now been rectified and the corrected article appears in this issue. The HTML and online PDF versions have also been rectified and now carry the correct name.

The authors would like to apologise for any inconvenience caused.

Originalsprache	Englisch
Zeitschrift	European Journal of Human Genetics
Jahrgang	20
Ausgabenummer	3
Seitenumfang	1
ISSN	1018-4813
DOIs	https://doi.org/10.1038/ejhg.2011.209
Publikationsstatus	Veröffentlicht - 01.03.2012

UN SDGs

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

SDG 3 – Gesundheit und Wohlergehen

Strategische Forschungsbereiche und Zentren

Querschnittsbereich: Medizinische Genetik

Dokumente

10.1038/ejhg.2011.209

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Braunholz, D., Hullings, M., Gil-Rodríguez, M. C., Fincher, C. T., Mallozzi, M. B., Loy, E., Albrecht, M., Kaur, M., Limon, J., Rampuria, A., Clark, D., Kline, A., Dalski, A., Eckhold, J., Tzschach, A., Hennekam, R., Gillessen-Kaesbach, G., Wierzba, J., Krantz, I. D., ... Kaiser, F. J. (2012). Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209). European Journal of Human Genetics, 20(3). https://doi.org/10.1038/ejhg.2011.209

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title = "Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209)",

abstract = "Since the publication of this article, the authors noted that NIPBL was mistyped in several places. This has now been rectified and the corrected article appears in this issue. The HTML and online PDF versions have also been rectified and now carry the correct name. The authors would like to apologise for any inconvenience caused.",

author = "Diana Braunholz and Melanie Hullings and Gil-Rodr{\'i}guez, \{Mar{\'i}a Concepcion\} and Fincher, \{Christopher T.\} and Mallozzi, \{Mark B.\} and Elizabeth Loy and Melanie Albrecht and Maninder Kaur and Janusz Limon and Abhinav Rampuria and Dinah Clark and Antonie Kline and Andreas Dalski and Juliane Eckhold and Andreas Tzschach and Raoul Hennekam and Gabriele Gillessen-Kaesbach and Jolanta Wierzba and Krantz, \{Ian D.\} and Deardorff, \{Matthew A.\} and Kaiser, \{Frank J.\}",

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day = "1",

doi = "10.1038/ejhg.2011.209",

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Braunholz, D, Hullings, M, Gil-Rodríguez, MC, Fincher, CT, Mallozzi, MB, Loy, E, Albrecht, M, Kaur, M, Limon, J, Rampuria, A, Clark, D, Kline, A, Dalski, A, Eckhold, J, Tzschach, A, Hennekam, R, Gillessen-Kaesbach, G, Wierzba, J, Krantz, ID, Deardorff, MA & Kaiser, FJ 2012, 'Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209)', European Journal of Human Genetics, Jg. 20, Nr. 3. https://doi.org/10.1038/ejhg.2011.209

Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209). / Braunholz, Diana; Hullings, Melanie; Gil-Rodríguez, María Concepcion et al.
in: European Journal of Human Genetics, Jahrgang 20, Nr. 3, 01.03.2012.

Publikation: Beiträge in Fachzeitschriften › Kommentare/Debatten

TY - JOUR

T1 - Erratum: Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction (European Journal of Human Genetics (2012) 20 (366) DOI:10.1038/ejhg.2011.209)

AU - Braunholz, Diana

AU - Hullings, Melanie

AU - Gil-Rodríguez, María Concepcion

AU - Fincher, Christopher T.

AU - Mallozzi, Mark B.

AU - Loy, Elizabeth

AU - Albrecht, Melanie

AU - Kaur, Maninder

AU - Limon, Janusz

AU - Rampuria, Abhinav

AU - Clark, Dinah

AU - Kline, Antonie

AU - Dalski, Andreas

AU - Eckhold, Juliane

AU - Tzschach, Andreas

AU - Hennekam, Raoul

AU - Gillessen-Kaesbach, Gabriele

AU - Wierzba, Jolanta

AU - Krantz, Ian D.

AU - Deardorff, Matthew A.

AU - Kaiser, Frank J.

PY - 2012/3/1

Y1 - 2012/3/1

N2 - Since the publication of this article, the authors noted that NIPBL was mistyped in several places. This has now been rectified and the corrected article appears in this issue. The HTML and online PDF versions have also been rectified and now carry the correct name. The authors would like to apologise for any inconvenience caused.

AB - Since the publication of this article, the authors noted that NIPBL was mistyped in several places. This has now been rectified and the corrected article appears in this issue. The HTML and online PDF versions have also been rectified and now carry the correct name. The authors would like to apologise for any inconvenience caused.

UR - https://www.scopus.com/pages/publications/84857164783

U2 - 10.1038/ejhg.2011.209

DO - 10.1038/ejhg.2011.209

M3 - Comments/Debates

AN - SCOPUS:84857164783

SN - 1018-4813

VL - 20

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 3

ER -