CFTR
NM_000492.4:p.F1052L
Ni Q et al.
Orphanet Journal of Rare Diseases, 2022
Khayat M et al.
Clinical Genetics, 2021
Bozdogan ST et al.
Genes, 2021
Şaşihüseyinoğlu AŞ et al.
The Turkish Journal of Pediatrics, 2019