CFTR mutations in the Algerian population
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health
Reference37 articles.
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4. An Algerian child homozygous for the M470V polymorphism and for a deletion of two nucleotides in exon 10 of the CFTR gene, shows severe cystic fibrosis symptoms;Loumi;Genet Couns,1992
5. Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: identification of two novel mutations;Messaoud;Eur J Hum Genet,1996
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