The Genetic Analysis of Cystic Fibrosis Patients with Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey

BACKGROUND: Cystic fibrosis, a pulmonary disease which is an autosomal recessive, inherited, multisystemic genetic disease commonly seen in the Caucasian race, is the most frequent cause of mortality and morbidity. So far, more than 2000 disease-causing gene variants have been found and this number...

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Detalles Bibliográficos
Autores principales: Erdoğan, Murat, Köse, Mehmet, Pekcan, Sevgi, Hangül, Melih, Balta, Burhan, Kiraz, Aslıhan, Akıncı Gönen, Gizem, Gül Zamani, Ayşe, Selman Yıldırım, Mahmut, Ramaslı Gürsoy, Tuğba, Ezgu, Fatih, Şişmanlar Eyüpoğlu, Tuğba, Tana Aslan, Ayse
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Trakya University School of Medicine 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880976/
https://www.ncbi.nlm.nih.gov/pubmed/34860163
http://dx.doi.org/10.5152/balkanmedj.2021.21199

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880976/
https://www.ncbi.nlm.nih.gov/pubmed/34860163
http://dx.doi.org/10.5152/balkanmedj.2021.21199

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