Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse-Sakati syndrome.
作者信息
Abdulla Mansoor C, Alazami Anas M, Alungal Jemshad, Koya Jassim M, Musambil Mohthash
机构信息
Department of Internal Medicine, Department of Radiodiagnosis, and Medical Biotechnology Central Research Lab, MES Medical College, Perinthalmanna 679 338,
出版信息
J Genet. 2015 Sep;94(3):489-92. doi: 10.1007/s12041-015-0544-7.
PMID:26440089
Abstract
摘要
Zotero 插件