Mutations in the canilicular multispecific organic anion transporter (cMOAT) gene, a novel ABC transporter, in patients with hyperbilirubinemia II/Dubin-Johnson syndrome

Human Molecular Genetics - Tập 7 Số 2 - Trang 203-207 - 1998
Morimasa Wada1, Shoichi Toh1, Ken Taniguchi1, Takanori Nakamura1, Takeshi Uchiumi1, Kimitoshi Kohno2, Ichiro Yoshida3, Akihiko Kimura3, Shotaro Sakisaka4, Yukihiko Adachi5, Michihiko Kuwano1
1Department of Biochemistry, Kyushu University School of Medicine, Fukuoka 812-82, Japan
2Department of Molecular Biology, University of Occupational and Environmental Health, Kitakyushu 807, Japan
3Department of Pediatrics and Child Health, Kurume University School of Medicine, Kurume 830, Japan
4Second Department of Medicine, Kurume University School of Medicine, Kurume 830, Japan
5Third Department of Internal Medicine, Mie University School of Medicine, Mie 514, Japan

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Human Molecular Genetics

Tập 7 Số 2

203-207

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