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Q36512067-06638913-4565-4028-ABF0-FCB3BEE91826
Q36512067-06638913-4565-4028-ABF0-FCB3BEE91826
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36512067-06638913-4565-4028-ABF0-FCB3BEE91826
Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4
P2860
Q36512067-06638913-4565-4028-ABF0-FCB3BEE91826
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36512067-06638913-4565-4028-ABF0-FCB3BEE91826
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wasDerivedFrom
ab82d6d02de2153225400098ebd44a3fa89b403b
P2860
A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)