Skip to main content
Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: Co-segregation of the c.489+3A>G variant with p.Cys1400Ter pathogenic CFTR mutation in Cyprus: prevalence and clinical implications

Fig. 2

Pedigrees of six non-related families of Cypriot descent with individuals bearing alleles that harboured in cis c.489+3A>G and p.Cys1400Ter in the CFTR gene. Red colour indicates the common haplotype found in all individuals carrying the in cis c.489+3A>G and p.Cys1400Ter; ST: sweat test; * individuals with cystic fibrosis; ** individuals with CFTR-related disorder; *** individuals with possible CFTR-related disorder

Back to article page

Orphanet Journal of Rare Diseases

ISSN: 1750-1172