Associated Papers
A frameshift mutation of TMPRSS3 in a Chinese family with non-syndromic hearing loss.
Liang J et al.
Frontiers in Pediatrics, 2022
TMPRSS3 Gene Variants With Implications for Auditory Treatment and Counseling.
Moon IS et al.
Frontiers in Genetics, 2021
Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families.
Sang S et al.
Frontiers in Genetics, 2019
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