A novelALDH5A1mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family-Reference-Cited by-同舟云学术

A novelALDH5A1mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family

Published:2013-07-04 Issue:8 Volume:161 Page:1915-1922
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Püttmann Lucia,Stehr Henning¹,Garshasbi Masoud²,Hu Hao²,Kahrizi Kimia³,Lipkowitz Bettina²,Jamali Payman⁴,Tzschach Andreas²,Najmabadi Hossein³,Ropers Hans-Hilger²,Musante Luciana²,Kuss Andreas W.

Affiliation:

1. Department of Vertebrate Genomics; Max Planck Institute for Molecular Genetics; Berlin; Germany

2. Department of Human Molecular Genetics; Max Planck Institute for Molecular Genetics; Berlin; Germany

3. Genetics Research Center; University of Social Welfare and Rehabilitation Sciences; Tehran; Iran

4. Shahroud Welfare Organization; Semnan; Iran

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36030/fullpdf

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