A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM) by Tozawa, Yusuke, Abdrabou, Shimaa Said Mohamed Ali, Nogawa-Chida, Natsuko, Nishiuchi, Ritsuo, Ishida, Toshiaki, Suzuki, Yuichi, Sano, Hideki, Kobayashi, Ryoji, Kishimoto, Kenji, Ohara, Osamu, Imai, Kohsuke, Naruto, Takuya, Kobayashi, Kunihiko, Ariga, Tadashi, Yamada, Masafumi

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