Novel variant p.E269K confirms causative role of PLS1 mutations in autosomal dominant hearing loss.

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Source: Clinical Genetics - August 20, 2019 Category: Genetics & Stem Cells Authors: Diaz-Horta O, Bademci G, Tokgoz-Yilmaz S, Guo S, Zafeer F, Sineni CJ, Duman D, Farooq A, Tekin M Tags: Clin Genet Source Type: research