CFTR gene analysis in cystic fibrosis patients: Detection of 91 % of molecular defects and identification of the novel mutation D979V

Annales de Genetique

Volumn 40, Issue 3, 1997, Pages 185-188

  Plouvier, E ^a   Cougoureux, E ^a   Sardet, A ^a   Tournier, G ^a   Aymard, P ^a   Feldmann, D ^a  

^a ARMAND TROUSSEAU HOSPITAL   (France)

Author keywords

Cystic Fibrosis; DGGE CFTR; Mutation D979V

Indexed keywords

TRANSMEMBRANE CONDUCTANCE REGULATOR;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CHILD; CHROMOSOME; CYSTIC FIBROSIS; DENATURING GRADIENT GEL ELECTROPHORESIS; DNA SEQUENCE; EXON; FEMALE; GENE; GENE MUTATION; HUMAN; HUMAN CELL; INTRON; MAJOR CLINICAL STUDY; MALE; TECHNIQUE;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; ELECTROPHORESIS, POLYACRYLAMIDE GEL; EXONS; FEMALE; HUMANS; INFANT; MALE; MIDDLE AGED; MUTATION;

EID: 0030685746     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (14)