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

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

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2015 Sep Others MC Abdulla, AM Alazami, J Alungal, JM Koya… - Journal of genetics, 2015 - Springer

Full Author : ['Abdulla, Mansoor C', 'Alazami, Anas M', 'Alungal, Jemshad', 'Koya, Jassim M', 'Musambil, Mohthash']
Journal Title : Journal of genetics
Chapter : Section3
Journal Year : 2015
Cited by : 12.0

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Keywords : ["novel compound heterozygous frameshift mutation", "familial indian case", "woodhousesakati syndrome"]
PubMed Link : https://link.springer.com/article/10.1007/s12041-015-0544-7
Google Scholar Link : https://scholar.google.com/scholar?cites=10598668170374332254&as_sdt=40005&sciodt=0,10&hl=en&num=20