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A rare cause of congenital diarrhea in a Turkish newborn: tufting enteropathy. [electronic resource] by
- Kahvecioğlu, Dilek
- Yıldız, Duran
- Kılıç, Atilla
- İnce-Alkan, Banu
- Erdeve, Ömer
- Kuloğlu, Zarife
- Atasay, Begüm
- Ensari, Arzu
- Yılmaz, Resul
- Arsan, Saadet
Producer: 20160324
In:
The Turkish journal of pediatrics vol. 56
Availability: No items available.
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2227.
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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). [electronic resource] 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
Producer: 20200519
In:
Clinical immunology (Orlando, Fla.) vol. 208
Availability: No items available.
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