Hasil Pencarian - Aradhna Mathur

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  1. 1
    Spinocerebellar ataxia type 10 (SCA10): Mutation analysis and common haplotype based inference suggest its rarity in Indian population

    Spinocerebellar ataxia type 10 (SCA10): Mutation analysis and common haplotype based inference suggest its rarity in Indian population oleh Divya Goel, Varun Suroliya, Uzma Shamim, Aradhna Mathur, Mohammed Faruq

    Diterbitkan 2019-12-01
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  2. 2
    A novel mutation in SGSH causing Sanfillipo type 3A Mucopolysaccharidoses in an Indian family

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

    Diterbitkan 2018-06-01
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