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Q35889891-10DF3AF9-8859-48C5-9B36-24DE9B664498
Q35889891-10DF3AF9-8859-48C5-9B36-24DE9B664498
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35889891-10DF3AF9-8859-48C5-9B36-24DE9B664498
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.
P2860
Q35889891-10DF3AF9-8859-48C5-9B36-24DE9B664498
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35889891-10DF3AF9-8859-48C5-9B36-24DE9B664498
rank
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type
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Statement
wasDerivedFrom
ed0358cd8b3deef2aef54e34c055269c62f2f4b2
P2860
High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays.