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Q33781512-AF45D0AA-0250-41E9-92C5-258DB34B0C40
Q33781512-AF45D0AA-0250-41E9-92C5-258DB34B0C40
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33781512-AF45D0AA-0250-41E9-92C5-258DB34B0C40
A novel PCFT gene mutation (p.Cys66LeufsX99) causing hereditary folate malabsorption
P2860
Q33781512-AF45D0AA-0250-41E9-92C5-258DB34B0C40
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33781512-AF45D0AA-0250-41E9-92C5-258DB34B0C40
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
c9866914ae29c664724e235a680e3e7ea4548289
P2860
A role for the proton-coupled folate transporter (PCFT-SLC46A1) in folate receptor-mediated endocytosis.