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  • Molecular assay reagents intended to identify mutations in the coagulation factor C homologue (COCH) gene, located at chromosome 14q12-q13, which encodes for a protein called cochlin that is involved in the structure of the inner ear. Mutations at this locus have been identified in patients with autosomal dominant nonsyndromic sensorineural 9 deafness (DFNA9); the exact effects of COCH mutations are unclear.
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