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Q44775711-2C714EB4-34E4-4694-AFA8-33500C06BDF1
Q44775711-2C714EB4-34E4-4694-AFA8-33500C06BDF1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44775711-2C714EB4-34E4-4694-AFA8-33500C06BDF1
A dominant mutation in the stereocilia-expressing gene TBC1D24 is a probable cause for nonsyndromic hearing impairment.
P2860
Q44775711-2C714EB4-34E4-4694-AFA8-33500C06BDF1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44775711-2C714EB4-34E4-4694-AFA8-33500C06BDF1
rank
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Statement
wasDerivedFrom
d9f3d97217b276c0520c57fc05783f9aa59ed469
P2860
DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3.