Association Study of IVS8TGmTn Polymorphism and Cystic Fibrosis Disease in a Tunisian Population

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Cystic fibrosis (CF) is the most common autosomal recessive disease in Caucasians, caused by mutation in cystic fibrosis transmembrane conductance regulator (CFTR). The analysis of some extra and intragenic markers within or closely linked to CFTR gene  is  useful  as  a  molecular  method  in  clinical  linkage  analysis.  Indeed, knowing that the molecular basis of CF is highly heterogeneous in Tunisian population is explained. For more:http://www.scitechnol.com/peer-review/association-study-of-ivs8tgmtn-polymorphism-and-cystic-fibrosis-disease-in-a-tunisian-population-s1mg.php?article_id=5921

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