Associated Papers
A novel splice-altering TNC variant (c.5247A > T, p.Gly1749Gly) in an Chinese family with autosomal dominant non-syndromic hearing loss.
He M et al.
Bmc Medical Genomics, 2024
Fluctuating hearing loss associated with a novel heterozygous variant in the TNC gene related to nonsyndromic hearing loss.
Castellanos-Acevedo MC et al.
Brazilian Journal of Otorhinolaryngology, 0
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