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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) |
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Titel: |
A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM) |
Auteur: |
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 |
Verschenen in: |
Clinical immunology |
Paginering: |
Jaargang 208 () nr. C pagina's p. |
Jaar: |
2019 |
Inhoud: |
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Uitgever: |
Elsevier Inc. |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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