1. A follow‐up study of a Chinese family with Waardenburg syndrome type II caused by a truncating mutation of MITF gene
   Shuzhi Yang et al, 2020, Molecular Genetics & Genomic Medicine CrossRef
2. A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options
   Nandita Sharma et al, 2023, Clinical Genetics CrossRef