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  1. 1
    Whole-exome sequencing identifies two novel ALMS1 mutations in Indian patients with Leber congenital amaurosis

    Whole-exome sequencing identifies two novel ALMS1 mutations in Indian patients with Leber congenital amaurosis by Natarajan N. Srikrupa, Sarangapani Sripriya, Suriyanarayanan Pavithra, Parveen Sen, Ravi Gupta, Sinnakaruppan Mathavan

    Published 2021-03-01
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  2. 2
    Homozygosity Mapping in Leber Congenital Amaurosis and Autosomal Recessive Retinitis Pigmentosa in South Indian Families.

    Homozygosity Mapping in Leber Congenital Amaurosis and Autosomal Recessive Retinitis Pigmentosa in South Indian Families. by Sundaramurthy Srilekha, Tharigopala Arokiasamy, Natarajan N Srikrupa, Vetrivel Umashankar, Swaminathan Meenakshi, Parveen Sen, Suman Kapur, Nagasamy Soumittra

    Published 2015-01-01
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