A novel mutation in exon 12 (Y569C) of the CFTR gene identified in a patient of Croatian origin.

Human mutation

Volumn 7, Issue 4, 1996, Pages 374-375

  Petreska, L ^a   Plaseska, D ^a   Koceva, S ^a   Stavljenic Rukavina A ^a   Efremov, G D ^a  

^a MACEDONIAN ACADEMY OF SCIENCES AND ARTS   (Macedonia)

Author keywords

[No Author keywords available]

Indexed keywords

CFTR PROTEIN, HUMAN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ARTICLE; CASE REPORT; CROATIA; CYSTIC FIBROSIS; ETHNOLOGY; EXON; FEMALE; GENETICS; HUMAN; MUTATION; PRESCHOOL CHILD; SINGLE STRAND CONFORMATION POLYMORPHISM;

CHILD, PRESCHOOL; CROATIA; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; EXONS; FEMALE; HUMANS; MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0029704018     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.1380070402     Document Type: Article

References (0)