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

Hepatology

Volumn 25, Issue 6, 1997, Pages 1539-1542

  Paulusma, Coen C ^a   Kool, Marcel ^b   Bosma, Piter J ^a   Scheffer, George L ^c   Borg, Frank Ter ^a   Scheper, Rik J ^c   Tytgat, Guido N J ^a   Borst, Piet ^b   Baas, Frank ^a   Oude Elferink, Ronald P J ^a  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

^b NETHERLANDS CANCER INSTITUTE   (Netherlands)

^c VU UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ANION TRANSPORT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CLINICAL FEATURE; DUBIN JOHNSON SYNDROME; FEMALE; GENE MUTATION; HUMAN; HUMAN TISSUE; HYPERBILIRUBINEMIA; MOLECULAR CLONING; PATHOGENESIS; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; ANION TRANSPORT PROTEINS; ANTIBODIES, MONOCLONAL; BASE SEQUENCE; CARRIER PROTEINS; DNA, COMPLEMENTARY; FEMALE; GENES; HUMANS; IMMUNOHISTOCHEMISTRY; JAUNDICE, CHRONIC IDIOPATHIC; LIVER; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; REFERENCE VALUES; TISSUE DISTRIBUTION;

EID: 0030994468     PISSN: 02709139     EISSN: None     Source Type: Journal    
DOI: 10.1002/hep.510250635     Document Type: Article

References (20)

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