A novel missense mutation in exon 16 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in CBAVD patients.

Human mutation

Volumn 7, Issue 2, 1996, Pages 182-

  Bienvenu, T ^a   Hubert, D ^a   Setbon, E ^a   Dusser, D ^a   Kaplan, J C ^a   Beldjord, C ^a  

^a CHU Cochin ^*  (France)

Author keywords

[No Author keywords available]

Indexed keywords

CFTR PROTEIN, HUMAN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ARTICLE; CONGENITAL MALFORMATION; EXON; GENETICS; HUMAN; MALE; POINT MUTATION; POLYMERASE CHAIN REACTION; VAS DEFERENS;

CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; EXONS; HUMANS; MALE; POINT MUTATION; POLYMERASE CHAIN REACTION; VAS DEFERENS;

EID: 18144437929     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1098-1004(1996)7:2<182::aid-humu19>3.3.co;2-y     Document Type: Article

References (0)