Congenital bilateral absence of vas deferens with a new missense mutation (P499A) in the CFTR gene

Author:

Arduino C.,Ferrone M.,Brusco A.,Garnerone S.,Fontana D.,Rolle L.,Carbonara AO

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference6 articles.

1. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens;Chillon;New EngI J Med,1995

2. Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA;Chu;Nat Genet,1993

3. Genetic history of cystic fibrosis mutations in Italy: I regional distribution;Rendine;Ann Hum Genet,1997

4. Development, multiplexing and application of ARMS test for corrimon mutations in the CFTR gene;Ferrie;Am J Hum Genet,1992

5. CFTR haplotype analysis reveals genetic heterogeneity in the etiology of congenital bilateral aplasia of the vas deferens;Rave-Harel;Am J Hum Genet,1995

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