Identification of a frameshift mutation (1609delCA) in exon 10 of the CFTR gene in seven Spanish cystic fibrosis patients
- 1 January 1992
- journal article
- mutation in-brief
- Published by Hindawi Limited in Human Mutation
- Vol. 1 (1) , 75-76
- https://doi.org/10.1002/humu.1380010113
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
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- CAGT Microsatellite alleles within the cystic fibrosis transmembrane conductance regulator (CFTR) gene are not generated by unequal crossingoverGenomics, 1991
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- A deletion of two nucleotides in exon 10 of the CFTR gene in a Soviet family with cystic fibrosis causing early infant deathGenomics, 1991
- 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
- Identification of the Cystic Fibrosis Gene: Genetic AnalysisScience, 1989