Spinocerebellar ataxia type 10 (SCA10): Mutation analysis and common haplotype based inference suggest its rarity in Indian population

by Divya Goel, Varun Suroliya, Uzma Shamim, Aradhna Mathur, Mohammed Faruq
Published 2019-12-01

A novel mutation in SGSH causing Sanfillipo type 3A Mucopolysaccharidoses in an Indian family

by Jyotsna Singh, P.K. Muhammad, Sweta Jain, Aradhna Mathur, Shaista Parveen, Aditi Joshi, Bharathram Uppili, C.V. Shaji, K.A. Kabeer, Suraj Menon, Mohammed Faruq
Published 2018-06-01