Novel Cystic Fibrosis mutation L1093P: functional analysis and possible Native American origin.

Human mutation

Volumn 15, Issue 2, 2000, Pages 208-

  Yee, K ^a   Robinson, C ^a   Hurlock, G ^a   Moss, R B ^a   Wine, J J ^a  

^a STANFORD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANION; CFTR PROTEIN, HUMAN; FORSKOLIN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ADULT; AMERICAN INDIAN; ARTICLE; CELL CULTURE; CYSTIC FIBROSIS; DRUG EFFECT; GENETIC TRANSFECTION; GENETICS; HUMAN; METABOLISM; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; POLYMERASE CHAIN REACTION; SINGLE STRAND CONFORMATION POLYMORPHISM; SITE DIRECTED MUTAGENESIS;

ADULT; ANIONS; BASE SEQUENCE; CELLS, CULTURED; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; FORSKOLIN; HUMANS; INDIANS, NORTH AMERICAN; MUTAGENESIS, SITE-DIRECTED; MUTATION, MISSENSE; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; TRANSFECTION;

EID: 0034134127     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(200002)15:2<208::AID-HUMU17>3.0.CO;2-6     Document Type: Article

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