A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption (Q42007772)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption |
scientific article |
Statements
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A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption (English)
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N Diop-Bove
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M Jain
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F Scaglia
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I D Goldman
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Identifiers
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