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Q24540491-95F89063-E753-4980-B12D-1D8190FAA409
Q24540491-95F89063-E753-4980-B12D-1D8190FAA409
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24540491-95F89063-E753-4980-B12D-1D8190FAA409
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness
P2860
Q24540491-95F89063-E753-4980-B12D-1D8190FAA409
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24540491-95F89063-E753-4980-B12D-1D8190FAA409
rank
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wasDerivedFrom
d532f787842542619dcbfec1d1c99b3cfcf5177d
P2860
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23