Mutational and clinical spectrum in a cohort of Chinese patients with hereditary nemaline myopathy.

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PMID: 32222963 [PubMed - as supplied by publisher]

Source: Clinical Genetics - March 28, 2020 Category: Genetics & Stem Cells Authors: Wang Q, Hu Z, Chang X, Yu M, Xie Z, Lv H, Zhang W, Xiong H, Yuan Y, Wang Z Tags: Clin Genet Source Type: research