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

Human Genome Variation
2021-03-29 | Journal article
Contributors: Natarajan N. Srikrupa; Sarangapani Sripriya; Suriyanarayanan Pavithra; Parveen Sen; Ravi Gupta; Sinnakaruppan Mathavan
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