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Q58694743-E381555B-25CF-4C6F-8C3A-6FEE491AC372
Q58694743-E381555B-25CF-4C6F-8C3A-6FEE491AC372
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Statement
http://www.wikidata.org/entity/statement/Q58694743-E381555B-25CF-4C6F-8C3A-6FEE491AC372
Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and homocystinuria
P2860
Q58694743-E381555B-25CF-4C6F-8C3A-6FEE491AC372
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58694743-E381555B-25CF-4C6F-8C3A-6FEE491AC372
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wasDerivedFrom
0320726e6fce75fbb4d53c216e7cf52b9df331c3
P2860
An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1