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Clinical and genetic analysis in Algerian cystic fibrosis patients

โœ Scribed by R. Boukari; L. Smati; K.N. Benhalla; C. Kaddache; O. Redjala; S. Touri; E. Girondon-Boulandet; M. Baghriche


Book ID
114412201
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
45 KB
Volume
11
Category
Article
ISSN
1526-0550

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Cystic fibrosis (CF) is an autosomal recessive disease characterized by obstruction and chronic infections of the respiratory tract and pancreatic insufficiency. The gene was cloned in 1989 and the most frequent mutation was shown to be the delta F508 mutation. During PGD, embryos obtained in vitro