A follow ‐up study of a Chinese family with Waardenburg syndrome type II caused by a truncating mutation of MITF gene

ConclusionThese findings offer a better understanding of the spectrum ofMITF mutations and highlight the necessity of continuous hearing assessment in WS patients.
Source: Molecular Genetics & Genomic Medicine - Category: Genetics & Stem Cells Authors: Tags: ORIGINAL ARTICLE Source Type: research
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