CFTR mutational screening by next‐generation sequencing reveals novel variants and a high carrier rate in a Middle Eastern population-Reference-Cited by-同舟云学术

CFTR mutational screening by next‐generation sequencing reveals novel variants and a high carrier rate in a Middle Eastern population

Published:2021-12-09 Issue: Volume: Page:
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Annals of Human Genetics

Author:

Farra Chantal¹²³,Awwad Johnny⁴,Hamadeh Lama²,Khoueiry Pierre⁵,Halawi Zeina²,Yazbeck Nadine¹,Daher Rose²,Souaid Mirna²³,Hamdar Layal⁴,Yammine Tony³,Yunis Khalid¹

Affiliation:

1. Department of Pediatrics American University of Beirut Medical Center Beirut Lebanon

2. Medical Genetics Unit, Department of pathology and Laboratory Medicine American University of Beirut Medical Center Beirut Lebanon

3. Medical Genetics Unit Saint Joseph University Beirut Lebanon

4. Department of Obstetrics and Gynecology American University of Beirut Medical Center Beirut Lebanon

5. Department of Biochemistry and Molecular Genetics American University of Beirut Medical Center Beirut Lebanon

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ahg.12450

Reference23 articles.

1. The road for survival improvement of cystic fibrosis patients in Arab countries

2. Cystic fibrosis: A worldwide analysis ofCFTR mutations?correlation with incidence data and application to screening

3. European best practice guidelines for cystic fibrosis neonatal screening

4. Survival and Complications of Beta-Thalassemia in Lebanon

5. Cystic fibrosis mortality and survival in the UK: 1947-2003

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