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

Abdulla, M. C., Alazami, A. M., Alungal, J., Koya, J. M., & Musambil, M. (2015). Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse–Sakati syndrome. Journal of Genetics, 94(3), 489–492. https://doi.org/10.1007/s12041-015-0544-7