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Q35993489-6316E79F-414F-4FFA-8981-C5C97A6F2BE5
Q35993489-6316E79F-414F-4FFA-8981-C5C97A6F2BE5
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Statement
http://www.wikidata.org/entity/statement/Q35993489-6316E79F-414F-4FFA-8981-C5C97A6F2BE5
A P425R mutation of the proton-coupled folate transporter causing hereditary folate malabsorption produces a highly selective alteration in folate binding.
P2860
Q35993489-6316E79F-414F-4FFA-8981-C5C97A6F2BE5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35993489-6316E79F-414F-4FFA-8981-C5C97A6F2BE5
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wasDerivedFrom
0fca53b5df877c71d67c3f62b34c2b65e609c6d6
P2860
Characterization of folate uptake by choroid plexus epithelial cells in a rat primary culture model.