Two new mutations (1811 + 1G-->C and Y569C) identified in the CFTR gene in patients of Macedonian and Croatian origin.

Acta medica Croatica : casopis Hravatske akademije medicinskih znanosti

Volumn 50, Issue 3, 1996, Pages 125-127

  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; CROATIA; CYSTIC FIBROSIS; EXON; FEMALE; GENETICS; HUMAN; INFANT; INTRON; MACEDONIA (REPUBLIC); POINT MUTATION; PRESCHOOL CHILD; SINGLE STRAND CONFORMATION POLYMORPHISM;

CHILD, PRESCHOOL; CROATIA; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; EXONS; FEMALE; HUMANS; INFANT; INTRONS; MACEDONIA (REPUBLIC); POINT MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0029682932     PISSN: 13300164     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)