Gene Mutations in the Egyptian Population: Current and Future Insights for Genetic Screening Strategy
Overview
Overview
Authors
Affiliations
Affiliations
Soon will be listed here.
Citing Articles
A comprehensive review of cystic fibrosis in Africa and Asia.
Bobbo K, Ahmad U, Chau D, Nordin N, Abdullah S Saudi J Biol Sci. 2023; 30(7):103685.
PMID: 37313453 PMC: 10258508. DOI: 10.1016/j.sjbs.2023.103685.
References
1.
Bombieri C, Claustres M, De Boeck K, Derichs N, Dodge J, Girodon E
. Recommendations for the classification of diseases as CFTR-related disorders. J Cyst Fibros. 2011; 10 Suppl 2:S86-102.
DOI: 10.1016/S1569-1993(11)60014-3.
View
2.
Wei S, Feldman G, Monaghan K
. Cystic Fibrosis testing among Arab-Americans. Genet Med. 2006; 8(4):255-8.
DOI: 10.1097/01.gim.0000214453.74456.f3.
View
3.
Lissens W, Mahmoud K, Seneca S, VAN Steirteghem A, Liebaers I
. Molecular analysis of the cystic fibrosis gene reveals a high frequency of the intron 8 splice variant 5T in Egyptian males with congenital bilateral absence of the vas deferens. Mol Hum Reprod. 1999; 5(1):10-3.
DOI: 10.1093/molehr/5.1.10.
View
4.
Wang X, Moylan B, Leopold D, Kim J, Rubenstein R, Togias A
. Mutation in the gene responsible for cystic fibrosis and predisposition to chronic rhinosinusitis in the general population. JAMA. 2000; 284(14):1814-9.
DOI: 10.1001/jama.284.14.1814.
View
5.
El-Seedy A, Pasquet M, Shafiek H, Morsi T, Kitzis A, Ladeveze V
. Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene mutations in North Egyptian population: implications for the genetic diagnosis in Egypt. Cell Mol Biol (Noisy-le-grand). 2017; 62(13):21-28.
DOI: 10.14715/cmb/2016.62.13.5.
View