megaloblastic anemia

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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-... 273 views
2
a clinical pandora: unusual manifestations of vitamin b12 deficiency
;Mary Anne Poovathingal;George George;Geeta Panicker;Somasundaran Abhilash
2015 almatourism DOI: 10.4103/2349-4220.17... 240 views

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clinical immunology (orlando, fla)
ISSN: 1521-7035 529 views

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deep intronic mutation hereditary folate malabsorption (hfm) proton-coupled folate transporter (pcft) slc46a1 hyperhomocysteinemia