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Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption

✍ Scribed by Daniel Sanghoon Shin; Kris Mahadeo; Sang Hee Min; Ndeye Diop-Bove; Peter Clayton; Rongbao Zhao; I. David Goldman

No coin nor oath required. For personal study only.

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