Novel autosomal dominant TMC1 variants linked to hearing loss: insight into protein-lipid interactions
Abstract Background TMC1, which encodes transmembrane channel-like protein 1, forms the mechanoelectrical transduction (MET) channel in auditory hair cells, necessary for auditory function. TMC1 variants are known to cause autosomal dominant (DFNA36) and autosomal recessive (DFNB7/11) non-syndromic...
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2023-12-01T00:00:00Z.
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