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    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 oleh Natarajan N. Srikrupa, Sarangapani Sripriya, Suriyanarayanan Pavithra, Parveen Sen, Ravi Gupta, Sinnakaruppan Mathavan

    Diterbitkan 2021-03-01
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