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Q28115631-2F490BF4-7418-41AF-8E8E-807115A49890
Q28115631-2F490BF4-7418-41AF-8E8E-807115A49890
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28115631-2F490BF4-7418-41AF-8E8E-807115A49890
Molecular Genetic Characterization of 151 Mut-Type Methylmalonic Aciduria Patients and Identification of 41 Novel Mutations in MUT
P2860
Q28115631-2F490BF4-7418-41AF-8E8E-807115A49890
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28115631-2F490BF4-7418-41AF-8E8E-807115A49890
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wasDerivedFrom
1762b302e88b5cec1c4f6d54ad1be9207b047c85
P2860
The cblD defect causes either isolated or combined deficiency of methylcobalamin and adenosylcobalamin synthesis.