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Q35993489-791082E0-C541-4360-A507-E346DDDC9B16
Q35993489-791082E0-C541-4360-A507-E346DDDC9B16
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35993489-791082E0-C541-4360-A507-E346DDDC9B16
A P425R mutation of the proton-coupled folate transporter causing hereditary folate malabsorption produces a highly selective alteration in folate binding.
P2860
Q35993489-791082E0-C541-4360-A507-E346DDDC9B16
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35993489-791082E0-C541-4360-A507-E346DDDC9B16
rank
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Statement
wasDerivedFrom
41904f6e423c1fd263aad55f76efa1e6caafda83
P2860
A role for the proton-coupled folate transporter (PCFT-SLC46A1) in folate receptor-mediated endocytosis.