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Q37332766-EB0DAD65-C0F7-434C-A230-DC71C0A7DD48
Q37332766-EB0DAD65-C0F7-434C-A230-DC71C0A7DD48
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37332766-EB0DAD65-C0F7-434C-A230-DC71C0A7DD48
Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31
P2860
Q37332766-EB0DAD65-C0F7-434C-A230-DC71C0A7DD48
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37332766-EB0DAD65-C0F7-434C-A230-DC71C0A7DD48
rank
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type
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Statement
wasDerivedFrom
7a18d6aca5ae108b9debf185dac3bf30700b799a
P2860
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p