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Q35993489-4978C41D-3F5F-4082-BC68-00653DBFDF94
Q35993489-4978C41D-3F5F-4082-BC68-00653DBFDF94
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http://www.wikidata.org/entity/statement/Q35993489-4978C41D-3F5F-4082-BC68-00653DBFDF94
A P425R mutation of the proton-coupled folate transporter causing hereditary folate malabsorption produces a highly selective alteration in folate binding.
P2860
Q35993489-4978C41D-3F5F-4082-BC68-00653DBFDF94
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35993489-4978C41D-3F5F-4082-BC68-00653DBFDF94
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wasDerivedFrom
41904f6e423c1fd263aad55f76efa1e6caafda83
P2860
Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption