Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption (Q34450436)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption |
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Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption (English)
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Andras Fiser
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Daniel Sanghoon Shin
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Sang Hee Min
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Laura Russell
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Rongbao Zhao
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I David Goldman
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30 August 2010
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116
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5162-5169
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