Identification of a novel homozygousTRAPPC9gene mutation causing non-syndromic intellectual disability, speech disorder, and secondary microcephaly-Reference-Cited by-同舟云学术

Identification of a novel homozygousTRAPPC9gene mutation causing non-syndromic intellectual disability, speech disorder, and secondary microcephaly

Published:2017-10-14 Issue:8 Volume:174 Page:839-845
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Abbasi Ansar A.¹,Blaesius Kathrin²³⁴^ORCID,Hu Hao⁵,Latif Zahid⁶,Picker-Minh Sylvie²³⁴⁷,Khan Muhammad N.⁶,Farooq Sundas¹,Khan Muzammil A.⁸,Kaindl Angela M.²³⁴⁷

Affiliation:

1. Department of Zoology; Mirpur University of Science and Technology (MUST); Mirpur Pakistan

2. Charité - Universitätsmedizin Berlin, Institute of Neuroanatomy and Cell Biology; Berlin Germany

3. Berlin Insitute of Health (BIH), Anna-Louisa-Karsch Strasse 2; 10178 Berlin Germany

4. Charité - Universitätsmedizin Berlin, Department of Pediatric Neurology; Berlin Germany

5. Guangzhou Women and Children's Medical Center; Guangzhou China

6. Department of Zoology; University of Azad Jammu and Kashmir Muzaffarabad; Muzaffarabad Pakistan

7. Department of Pediatric Neurology; Charité-Universitätsmedizin Berlin; Berlin Germany

8. Gomal Centre of Biochemistry and Biotechnology (GCBB); Gomal University; Dera Ismail Khan Pakistan

Funder

Deutsche Forschungsgemeinschaft

Higher Education Commission, Pakistan

Berlin Institute of Health

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

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