Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse-Sakati syndrome

Journal article

Peer reviewed

Mansoor C. Abdulla, Anas M. Alazami, Jemshad Alungal, Jassim M. Koya and Mohthash Musambil

Journal of genetics, Vol.94(3), pp.489-492

01/09/2015

PMID: 26440089

Abstract

Genetics & Heredity

Life Sciences & Biomedicine

Science & Technology

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Title: Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse-Sakati syndrome
Creators - without role: Mansoor C. Abdulla - College Station Medical Center
Anas M. Alazami - King Faisal Specialist Hospital & Research Centre
Jemshad Alungal - College Station Medical Center
Jassim M. Koya - College Station Medical Center
Mohthash Musambil - College Station Medical Center
Publication Details: Journal of genetics, Vol.94(3), pp.489-492
Publisher: Indian Acad Sciences
Number of pages: 4
Identifiers: 9948103908331
Academic Unit: King Saud University
Language: English
Resource Type: Journal article