Whole exome-sequencing identifies rare pathogenic and candidate variants in sporadic Chinese Han deaf patients.

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PMID: 31486067 [PubMed - as supplied by publisher]

Source: Clinical Genetics - September 3, 2019 Category: Genetics & Stem Cells Authors: Zou S, Mei X, Yang W, Zhu R, Yang T, Hu H Tags: Clin Genet Source Type: research