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Q34560178-0E5EBC1B-E0D6-46BE-B241-5A0ADF5FE405
Q34560178-0E5EBC1B-E0D6-46BE-B241-5A0ADF5FE405
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34560178-0E5EBC1B-E0D6-46BE-B241-5A0ADF5FE405
Clinical, Biochemical, and Molecular Presentation in a Patient with the cblD-Homocystinuria Inborn Error of Cobalamin Metabolism.
P2860
Q34560178-0E5EBC1B-E0D6-46BE-B241-5A0ADF5FE405
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34560178-0E5EBC1B-E0D6-46BE-B241-5A0ADF5FE405
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Statement
wasDerivedFrom
2cea647fc4d440a3a752d49c457434fd8893016d
P2860
An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1