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Q28298001-59D822B3-C3C9-42DF-B515-A2C5D3A3C1C4
Q28298001-59D822B3-C3C9-42DF-B515-A2C5D3A3C1C4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28298001-59D822B3-C3C9-42DF-B515-A2C5D3A3C1C4
An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1
P2860
Q28298001-59D822B3-C3C9-42DF-B515-A2C5D3A3C1C4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28298001-59D822B3-C3C9-42DF-B515-A2C5D3A3C1C4
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type
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wasDerivedFrom
71bdb323389ba4f63b34a15420fb9c6f7b48a649
P2860
Cobalamin C defect: natural history, pathophysiology, and treatment.