儿童Alport综合征合并GJB2基因突变1例分析并文献复习
成艳辉, 包瑛, 骞佩, 黄惠梅
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
临床荟萃
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2022, (4): 354
-357
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DOI: 10.3969/j.issn.1004-583X.2022.04.013
