CFTR mutations in the Algerian population

Author:

Loumi O.,Ferec C.,Mercier B.,Creff J.,Fercot B.,Denine R.,Grangaud J.P.

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Reference37 articles.

1. Identification of the cystic fibrosis gene: genetic analysis;Kerem;Science,1989

2. Identification of the cystic fibrosis gene: chromosome walking and jumping;Rommens;Science,1989

3. Identification of a new frameshift mutation and a duplication polymorphism in the CFTR gene in the Algerian population;Cuppens;Hum Mol Genet,1992

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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