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Novel Mutations and Mutation Combinations of TMPRSS3 Cause Various Phenotypes in One Chinese Family with Autosomal Recessive Hearing Impairment.Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population.A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family.Prelingual Sensorineural Hearing Loss Caused by a Novel GJB2 Dominant Mutation in a Chinese Family
P50
description
researcher (ORCID 0000-0003-4305-1206)
@en
name
Xue Gao
@en
type
label
Xue Gao
@en
prefLabel
Xue Gao
@en
P31
P496
0000-0003-4305-1206