Missense variations in the cystic fibrosis gene: heteroduplex formation in the F508C mutation
- PMID: 1384326
- PMCID: PMC1682853
Missense variations in the cystic fibrosis gene: heteroduplex formation in the F508C mutation
Comment in
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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.Am J Hum Genet. 1993 Jul;53(1):292-3. Am J Hum Genet. 1993. PMID: 7686336 Free PMC article. No abstract available.
Comment on
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Benign missense variations in the cystic fibrosis gene.Am J Hum Genet. 1990 Oct;47(4):611-5. Am J Hum Genet. 1990. PMID: 1977306 Free PMC article.
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