Corrigendum to "Hyperphosphatasia With Seizures, Neurologic Deficit, and Characteristic Facial Features: Five New Patients With Mabry Syndrome" Am J Med Genet 152A: 1661-1669

Miles D. Thompson; Marjan M. Nezarati; Gabriele Gillessen-Kaesbach; Peter Meinecke; Roberto Mendoza-Londono; Etienne Mornet; Isabelle Brun-Heath; Catherine Prost Squarcioni; Laurence Legeai-Mallet; Arnold Munnich; David E.C. Cole

doi:10.1002/ajmg.a.33680

Corrigendum to "Hyperphosphatasia With Seizures, Neurologic Deficit, and Characteristic Facial Features: Five New Patients With Mabry Syndrome" Am J Med Genet 152A: 1661-1669

Miles D. Thompson, Marjan M. Nezarati, Gabriele Gillessen-Kaesbach, Peter Meinecke, Roberto Mendoza-Londono, Etienne Mornet, Isabelle Brun-Heath, Catherine Prost Squarcioni, Laurence Legeai-Mallet, Arnold Munnich, David E.C. Cole^*

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

Institut für Humangenetik

1 Zitat (Scopus)

Originalsprache	Englisch
Zeitschrift	American Journal of Medical Genetics, Part A
Jahrgang	155
Ausgabenummer	5
Seiten (von - bis)	1215
Seitenumfang	1
ISSN	1552-4825
DOIs	https://doi.org/10.1002/ajmg.a.33680
Publikationsstatus	Veröffentlicht - 05.2011

UN SDGs

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SDG 3 – Gesundheit und Wohlergehen

Strategische Forschungsbereiche und Zentren

Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)

Dokumente

10.1002/ajmg.a.33680

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Thompson, M. D., Nezarati, M. M., Gillessen-Kaesbach, G., Meinecke, P., Mendoza-Londono, R., Mornet, E., Brun-Heath, I., Squarcioni, C. P., Legeai-Mallet, L., Munnich, A., & Cole, D. E. C. (2011). Corrigendum to "Hyperphosphatasia With Seizures, Neurologic Deficit, and Characteristic Facial Features: Five New Patients With Mabry Syndrome" Am J Med Genet 152A: 1661-1669. American Journal of Medical Genetics, Part A, 155(5), 1215. https://doi.org/10.1002/ajmg.a.33680

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title = "Corrigendum to {"}Hyperphosphatasia With Seizures, Neurologic Deficit, and Characteristic Facial Features: Five New Patients With Mabry Syndrome{"} Am J Med Genet 152A: 1661-1669",

author = "Thompson, \{Miles D.\} and Nezarati, \{Marjan M.\} and Gabriele Gillessen-Kaesbach and Peter Meinecke and Roberto Mendoza-Londono and Etienne Mornet and Isabelle Brun-Heath and Squarcioni, \{Catherine Prost\} and Laurence Legeai-Mallet and Arnold Munnich and Cole, \{David E.C.\}",

year = "2011",

month = may,

doi = "10.1002/ajmg.a.33680",

language = "English",

volume = "155",

pages = "1215",

journal = "American Journal of Medical Genetics, Part A",

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Thompson, MD, Nezarati, MM, Gillessen-Kaesbach, G, Meinecke, P, Mendoza-Londono, R, Mornet, E, Brun-Heath, I, Squarcioni, CP, Legeai-Mallet, L, Munnich, A & Cole, DEC 2011, 'Corrigendum to "Hyperphosphatasia With Seizures, Neurologic Deficit, and Characteristic Facial Features: Five New Patients With Mabry Syndrome" Am J Med Genet 152A: 1661-1669', American Journal of Medical Genetics, Part A, Jg. 155, Nr. 5, S. 1215. https://doi.org/10.1002/ajmg.a.33680

Corrigendum to "Hyperphosphatasia With Seizures, Neurologic Deficit, and Characteristic Facial Features: Five New Patients With Mabry Syndrome" Am J Med Genet 152A: 1661-1669. / Thompson, Miles D.; Nezarati, Marjan M.; Gillessen-Kaesbach, Gabriele et al.
in: American Journal of Medical Genetics, Part A, Jahrgang 155, Nr. 5, 05.2011, S. 1215.

Publikation: Beiträge in Fachzeitschriften › Kommentare/Debatten

TY - JOUR

T1 - Corrigendum to "Hyperphosphatasia With Seizures, Neurologic Deficit, and Characteristic Facial Features: Five New Patients With Mabry Syndrome" Am J Med Genet 152A: 1661-1669

AU - Thompson, Miles D.

AU - Nezarati, Marjan M.

AU - Gillessen-Kaesbach, Gabriele

AU - Meinecke, Peter

AU - Mendoza-Londono, Roberto

AU - Mornet, Etienne

AU - Brun-Heath, Isabelle

AU - Squarcioni, Catherine Prost

AU - Legeai-Mallet, Laurence

AU - Munnich, Arnold

AU - Cole, David E.C.

PY - 2011/5

Y1 - 2011/5

UR - https://www.scopus.com/pages/publications/79955004070

U2 - 10.1002/ajmg.a.33680

DO - 10.1002/ajmg.a.33680

M3 - Comments/Debates

AN - SCOPUS:79955004070

SN - 1552-4825

VL - 155

SP - 1215

JO - American Journal of Medical Genetics, Part A

JF - American Journal of Medical Genetics, Part A

IS - 5

ER -