Usher 1C is a human gene. Recessive alleles of this gene are responsible for type 1C Usher syndrome and nonsyndromic deafness.
The official name of the gene Usher 1C is “Usher syndrome 1C (autosomal recessive, severe).” USH1C is the gene's official symbol. The USH1C gene is also known by other names, listed in the Other Names section, below.
Read more about Usher 1C: Function, Other Names
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