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

Natarajan N Srikrupa1, Sarangapani Sripriya1, Suriyanarayanan Pavithra2

  • 1SNONGC Department of Genetics and Molecular Biology, Vision Research Foundation, Sankara Nethralaya, Chennai, India.

Human Genome Variation
|March 30, 2021
PubMed

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