[Clinical hearing phenotypes analysis of GJB2 gene p.V37I homozygote and compound heterozygote mutation in infants].
Year: 2024
Type: other
Abstract: gene p. V37I homozygote and compound heterozygote mutation, mainly mild hearing loss. There was no difference in the probability of hearing loss and the distribution of hearing loss degree between the two groups. Patients with p. V37I homozygous and compound heterozygous mutation currently diagnosed as normal hearing need continuous clinical follow-up.
Source: PubMed
Authors: Yu Ruan, Cheng Wen, Xiaohua Cheng, Wei Zhang, Jinge Xie, Yue Li, Lin Deng, Lihui Huang
Institutions: Beijing Tongren Hospital, Capital Medical University
Language: English
Subfield: Sensory Systems
Field: Neuroscience
Domain: Life Sciences
Open Access status: green
OpenAlex ID: W4404836721