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
- PMID: 7686336
- PMCID: PMC1682253
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
Comment in
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A healthy male with compound and double heterozygosities for delta F508, F508C, and M47OV in exon 10 of the cystic fibrosis gene.Am J Hum Genet. 1994 Feb;54(2):384-5. Am J Hum Genet. 1994. PMID: 7508183 Free PMC article. No abstract available.
Comment on
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Missense variations in the cystic fibrosis gene: heteroduplex formation in the F508C mutation.Am J Hum Genet. 1992 Nov;51(5):1173-4. Am J Hum Genet. 1992. PMID: 1384326 Free PMC article. No abstract available.
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