NDST1missense mutations in autosomal recessive intellectual disability-Reference-Cited by-同舟云学术

NDST1missense mutations in autosomal recessive intellectual disability

Published:2014-08-14 Issue:11 Volume:164 Page:2753-2763
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Reuter Miriam S.¹,Musante Luciana²,Hu Hao²,Diederich Stefan³,Sticht Heinrich⁴,Ekici Arif B.¹,Uebe Steffen¹,Wienker Thomas F.²,Bartsch Oliver³,Zechner Ulrich³,Oppitz Cornelia⁵,Keleman Krystyna⁵⁶,Jamra Rami Abou¹,Najmabadi Hossein⁷⁸,Schweiger Susann³,Reis André¹,Kahrizi Kimia⁷

Affiliation:

1. Institute of Human Genetics; Friedrich-Alexander-Universität Erlangen-Nürnberg; Erlangen Germany

2. Max-Planck-Institute for Molecular Genetics; Dept. Human Molecular Genetics; Berlin Germany

3. Institute of Human Genetics; University Medical Center of the Johannes Gutenberg University Mainz; Mainz Germany

4. Institute of Biochemistry; Friedrich-Alexander-Universität Erlangen-Nürnberg; Erlangen Germany

5. Research Institute of Molecular Pathology; Vienna Austria

6. Janelia Farm Research Campus; Howard Hughes Medical Institute; Ashburn Virginia

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

8. Kariminejad-Najmabadi Pathology & Genetics Center Tehran; Tehran Iran

Funder

MRNET consortium, the EU FP 7 project GENCODYS

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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