slc46a1

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A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM).

Tozawa, Yusuke;Abdrabou, Shimaa Said Mohamed Ali;Nogawa-Chida, Natsuko;Nishiuchi, Ritsuo;Ishida, Tos...

2019 clinical immunology (orlando, fla) DOI: S1521-6616(19)30241-... 259 views

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clinical immunology (orlando, fla)

ISSN: 1521-7035 479 views

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deep intronic mutation hereditary folate malabsorption (hfm) megaloblastic anemia proton-coupled folate transporter (pcft)