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Q51904642-99CDDBA6-A354-41D2-9372-68DA2E7B5D86
Q51904642-99CDDBA6-A354-41D2-9372-68DA2E7B5D86
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http://www.wikidata.org/entity/statement/Q51904642-99CDDBA6-A354-41D2-9372-68DA2E7B5D86
A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders.
P2860
Q51904642-99CDDBA6-A354-41D2-9372-68DA2E7B5D86
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51904642-99CDDBA6-A354-41D2-9372-68DA2E7B5D86
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wasDerivedFrom
f4ec5ed0ea9676933a92ddc69a68d71e8a2aaac0
P2860
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)