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Q35882731-7EFFB98B-4E7F-44DF-81C7-FC8C245CBBC1
Q35882731-7EFFB98B-4E7F-44DF-81C7-FC8C245CBBC1
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Statement
http://www.wikidata.org/entity/statement/Q35882731-7EFFB98B-4E7F-44DF-81C7-FC8C245CBBC1
A mutation causing Alport syndrome with tardive hearing loss is common in the western United States.
P2860
Q35882731-7EFFB98B-4E7F-44DF-81C7-FC8C245CBBC1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35882731-7EFFB98B-4E7F-44DF-81C7-FC8C245CBBC1
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wasDerivedFrom
69c687af6dab52ee9ad1dfdfd1c024087da8adfd
P2860
Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome