High Frequency of the R117H Cystic Fibrosis Mutation in Patients with Congenital Absence of the Vas Deferens

Radj Gervais; Viviane Dumur; Jean-Marc Rigot; Jean-Jacques Lafitte; Philippe Roussel; Mireille Claustres; Jacques Demaille

Journal ArticleOPEN ACCESS

High Frequency of the R117H Cystic Fibrosis Mutation in Patients with Congenital Absence of the Vas Deferens

Gervais R
Dumur V
Rigot J
et al.

New England Journal of Medicine (1993) 328(6) 446-447

DOI: 10.1056/nejm199302113280619

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Abstract

To the Editor: We have previously described an increased frequency of the δF508 mutation of the cystic fibrosis gene in a group of patients with congenital absence of the vas deferens1. This sugges...

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Gervais, R., Dumur, V., Rigot, J.-M., Lafitte, J.-J., Roussel, P., Claustres, M., & Demaille, J. (1993). High Frequency of the R117H Cystic Fibrosis Mutation in Patients with Congenital Absence of the Vas Deferens. New England Journal of Medicine, 328(6), 446–447. https://doi.org/10.1056/nejm199302113280619

High Frequency of the R117H Cystic Fibrosis Mutation in Patients with Congenital Absence of the Vas Deferens

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