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Q34452951-1A4F83B2-0CC2-4A50-B103-56F2AA7964B4
Q34452951-1A4F83B2-0CC2-4A50-B103-56F2AA7964B4
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http://www.wikidata.org/entity/statement/Q34452951-1A4F83B2-0CC2-4A50-B103-56F2AA7964B4
Novel mutations in the USH1C gene in Usher syndrome patients.
P2860
Q34452951-1A4F83B2-0CC2-4A50-B103-56F2AA7964B4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34452951-1A4F83B2-0CC2-4A50-B103-56F2AA7964B4
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wasDerivedFrom
89f05fd5c062e7059ec75c814b821d86cdec349e
P2860
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.