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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Demographic characteristics, clinical and laboratory features, and the distribution of pathogenic variants in the CFTR gene in the Cypriot cystic fibrosis (CF) population demonstrate the utility of a national CF patient registry

Fig. 1

Frequency of CFTR mutations in on all CF alleles in the Cypriot population. CFTR mutations are presented in legacy nomenclature; the listed variant frequencies are present both in the classical forms of the disease and cases with CFTR-related diseases

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172