Clinical characteristics and genotype analysis of the child with Alport syndrome with GJB2 gene mutation-induced deafness: A case report and literature review
Cheng Yanhui, Bao Ying, Qian Pei, Huang Huimei
Clinical Focus . 2022, (4): 354 -357 .  DOI: 10.3969/j.issn.1004-583X.2022.04.013