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DFNB59

Official Full Name
pejvakin
Organism
Homo sapiens
GeneID
494513
Background
The protein encoded by this gene is a member of the gasdermin family, a family which is found only in vertebrates. The encoded protein is required for the proper function of auditory pathway neurons. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59). [provided by RefSeq, Dec 2008]
Synonyms
PJVK; DFNB59;

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