Correction to “Evaluation of clinical and genetic characteristics of cystic fibrosis patients in the Southeastern Anatolia of Turkey”

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Abstract

Arik E, Keskin O, Korkmaz M, Şen V, Hangül M, Cesur M, et al. Evaluation of clinical and genetic characteristics of cystic fibrosis patients in the Southeastern Anatolia of Turkey. Pediatr Int. 2025; 67:e70197. https://doi.org/10.1111/ped.70197 The mutations identified in the study cohort, including the variant c.3874-3C>G, detected in four patients, are reported in Table 2. However, upon re-evaluation of the genome assembly (hg38), the intronic nucleotide located three bases upstream of c.3874 is T, not C. Therefore, the correct nomenclature of this variant should be c.3874-3T>G. The correct version of Table 2 is provided below. We apologize for this error.

Fields of Study & Subjects

Cystic Fibrosis Research Advances Genomics and Rare Diseases Genetic and Kidney Cyst Diseases

Publication details

Journal / source
Pediatrics International
Volume
68
Issue
1
Pages
e70360–e70360
Publication date
1 January 2026
Language
EN