A mutation which disrupts the hydrophobic core of the signal peptide of bilirubin UDP-glucuronosyltransferase, an endoplasmic reticulum membrane protein, causes Crigler-Najjar type II

FEBS Letters

Volumn 390, Issue 3, 1996, Pages 294-298

  Seppen, Jurgen ^a   Steenken, Edmee ^a   Lindhout, Dick ^b   Bosma, Piter J ^a   Oude Elferink, Ronald P J ^a  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

^b ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

Bilirubin; Crigler Najjar; Endoplasmic reticulum; Signal peptide; UDP glucuronosyltransferase

Indexed keywords

GLUCURONOSYLTRANSFERASE;

ANIMAL CELL; ARTICLE; CELL STRAIN COS1; CONTROLLED STUDY; CRIGLER NAJJAR SYNDROME; DNA TRANSFECTION; ENDOPLASMIC RETICULUM; GENE EXPRESSION; GENETIC ANALYSIS; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; MUTATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN PROCESSING; RNA TRANSLATION;

EID: 0030605859     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/0014-5793(96)00677-1     Document Type: Article

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