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

J Genet

Department of Internal Medicine, Department of Radiodiagnosis, and Medical Biotechnology Central Research Lab, MES Medical College, Perinthalmanna 679 338,

Published: September 2015

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Source
http://dx.doi.org/10.1007/s12041-015-0544-7DOI Listing

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