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Q21202842-1ACFDE25-DA3B-4CEF-83D2-7374E445EE81
Q21202842-1ACFDE25-DA3B-4CEF-83D2-7374E445EE81
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http://www.wikidata.org/entity/statement/Q21202842-1ACFDE25-DA3B-4CEF-83D2-7374E445EE81
EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness.
P2860
Q21202842-1ACFDE25-DA3B-4CEF-83D2-7374E445EE81
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21202842-1ACFDE25-DA3B-4CEF-83D2-7374E445EE81
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type
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wasDerivedFrom
bcbb0e30cb555a558f52693db9ee74a1f0a33d4a
P2860
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31