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

Human Molecular Genetics

Volumn 7, Issue 2, 1998, Pages 203-207

  Wada, Morimasa ^a   Toh, Satoshi ^a   Taniguchi, Ken ^a   Nakamura, Takanori ^a   Uchiumi, Takeshi ^a   Kohno, Kimitoshi ^b   Yoshida, Ichiro ^c   Kimura, Akihiko ^c   Sakisaka, Shotaro ^c   Adachi, Yukihiko ^d   Kuwano, Michihiko ^a  

^a KYUSHU UNIVERSITY   (Japan)

^b UNIVERSITY OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH   (Japan)

^c KURUME UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^d MIE UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; ANION; ANION TRANSPORT PROTEIN; CARRIER PROTEIN; COMPLEMENTARY DNA;

ANION TRANSPORT; ARTICLE; CASE REPORT; CONTROLLED STUDY; DUBIN JOHNSON SYNDROME; GENE DELETION; HUMAN; HUMAN TISSUE; MISSENSE MUTATION; PRIORITY JOURNAL; AMINO ACID SEQUENCE; FEMALE; GENETICS; JAUNDICE; MALE; MIDDLE AGED; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; POINT MUTATION; POLYMERASE CHAIN REACTION; RNA SPLICING;

AMINO ACID SEQUENCE; ANION TRANSPORT PROTEINS; BASE SEQUENCE; CARRIER PROTEINS; DNA MUTATIONAL ANALYSIS; DNA, COMPLEMENTARY; FEMALE; HUMANS; JAUNDICE, CHRONIC IDIOPATHIC; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; POINT MUTATION; POLYMERASE CHAIN REACTION; RNA SPLICING; SEQUENCE DELETION;

EID: 6844250107     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/7.2.203     Document Type: Article

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