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

被引：0

作者：

MANSOOR C. ABDULLA

ANAS M. ALAZAMI

JEMSHAD ALUNGAL

JASSIM M. KOYA

MOHTHASH MUSAMBIL

机构：

[1] MES Medical College,Department of Internal Medicine

[2] King Faisal Specialist Hospital and Research Center,Department of Genetics

[3] MES Medical College,Department of Radiodiagnosis

[4] MES Medical College,Medical Biotechnology Central Research Lab

来源：

Journal of Genetics | 2015年 / 94卷

关键词：

Woodhouse–Sakati syndrome; Indian family;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

页码：489 / 492

页数：3