Clinical, Pathologic, and Genetic Features of Neonatal Dubin-Johnson Syndrome: A Multicenter Study in Japan

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

Sue Richards, Nazneen Aziz, Sherri J. Bale et al. · Genetics in Medicine · 2015 · 32.2K citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome

Coen C. Paulusma, Marcel Kool, Piter J. Bosma et al. · Hepatology · 1997 · 557 citations · Full text

Medicine, Genetics, Molecular Genetics +17

CHRONIC IDIOPATHIC JAUNDICE WITH UNIDENTIFIED PIGMENT IN LIVER CELLS

I. N. Dubin, Frank B. Johnson · Medicine · 1954 · 454 citations

Medicine, Pathobiology, Pathology +15

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

Morimasa Wada · Human Molecular Genetics · 1998 · 260 citations · Full text

Life Sciences, Molecular Biology, Molecular Genetics +13

Trafficking and functional defects by mutations of the ATP-binding domains in MRP2 in patients with Dubin-Johnson syndrome

Kenkichi Hashimoto, Takeshi Uchiumi, Toshikazu Konno et al. · Hepatology · 2002 · 118 citations · Full text

Life Sciences, Biochemistry, Cell Biology +13