Compound heterozygosity for the delta F508 and F508C cystic fibrosis transmembrane conductance regulator (CFTR) mutations in a patient with congenital bilateral aplasia of the vas deferens.
- 1 July 1993
- Vol. 53 (1) , 292-3
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Missense variations in the cystic fibrosis gene: heteroduplex formation in the F508C mutation.1992
- Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis.1992
- Congenital Absence of the Vas DeferensNew England Journal of Medicine, 1990
- Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene.Proceedings of the National Academy of Sciences, 1990
- BENIGN MISSENSE VARIATIONS IN THE CYSTIC-FIBROSIS GENE1990