New genetics of inheritable jaundice and cholestatic liver disease

Lancet

Volumn 352, Issue 9122, 1998, Pages 82-83

  Arias, I M ^a  

^a TUFTS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALAGILLE SYNDROME; CHOLESTATIC HEPATITIS; CRIGLER NAJJAR SYNDROME; DUBIN JOHNSON SYNDROME; FAMILIAL DISEASE; GENETICS; GILBERT DISEASE; HUMAN; JAUNDICE; MOLECULAR GENETICS; PRIORITY JOURNAL; SHORT SURVEY;

EID: 0032508289     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(98)85004-6     Document Type: Note

References (9)

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3. CC Paulusma M Kool PJ Bosma A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome Hepatology 25 1997 1539 1542
4. LN Bull van Eijk Pawlikowska L A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis Nat Genet 18 1998 219 224
5. SS Strautnieks AF Kagalwalla MS Tanner Identification of a locus for progressive familial intrahepatic cholestasis PFIC2 on chromosome 2p24 Am J Hum Gen 61 1997 630 633
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9. T Oda AG Elkahloun BL Pike Mutations in human jagged 1 gene are responsible for Alagille syndrome Nat Genet 16 1997 235 242