A missense mutation (F87L) in exon 3 of the cystic fibrosis transmembrane conductance regulator gene
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference13 articles.
1. (1989) Cystic fibrosis. In (eds): The metabolic Basis of Inherited Disease, 6th ed. New York: McGraw-Hill, pp 2649-2680.
2. Psoralen-modified oligonucleotide primers improve detection of mutations by denaturing gradient gel electrophoresis and provide an alternative to GC-clamping
3. A cross-species analysis of the cystic fibrosis transmembrane conductance regulator. Potential functional domains and regulatory sites.
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