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: Shuzhi Yang,
Cuicui Wang,
Chengyong Zhou,
DongYang Kang,
Xin Zhang,
Huijun Yuan Tags: ORIGINAL ARTICLE Source Type: research