A novel CFTR disease-associated mutation causes addition of an extra N-linked oligosaccharide

Glycoconjugate Journal

Volumn 17, Issue 11, 2000, Pages 807-813

  Hämmerle, Marcus M ^a   Aleksandrov, Andrei A ^a   Chang, Xiu Bao ^a   Riordan, John R ^a  

^a MAYO CLINIC   (United States)

Author keywords

CFTR; Glycosylation; Ion channel; Mutation

Indexed keywords

AMINO ACID; ASPARAGINE LINKED OLIGOSACCHARIDE; CALNEXIN; CHAPERONE; CHLORIDE CHANNEL; CHLORIDE ION; OLIGOSACCHARIDE; OLIGOSACCHARYLTRANSFERASE; TRANSFERASE; TRANSMEMBRANE CONDUCTANCE REGULATOR; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CARBOXY TERMINAL SEQUENCE; CELL MEMBRANE; CHLORIDE TRANSPORT; CONTROLLED STUDY; CYSTIC FIBROSIS; CYTOPLASM; ENDOPLASMIC RETICULUM; GENE MUTATION; MEMBRANE BINDING; MISSENSE MUTATION; NONHUMAN; POROSITY; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

AMINO ACID SEQUENCE; CALCIUM-BINDING PROTEINS; CALNEXIN; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; HUMANS; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTATION; OLIGOSACCHARIDES; PROTEIN BINDING; PROTEIN PROCESSING, POST-TRANSLATIONAL;

ANIMALIA;

EID: 0034435098     PISSN: 02820080     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1010992827511     Document Type: Article

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