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GENATLAS PHENOTYPE

last update : 30/03/2006

Symbol	DFNB16
Location	15q15.3
Name	neurosensory deafness 16
Corresponding gene	STRC
related resource	Genetics hearing impairment
Main clinical features	non syndromic, severe or profound, Pakistani and Middle East kindreds
Genetic determination	autosomal recessive
Function/system disorder	ear
Type	disease

Gene product

Name	stereocilin