A deletion of two nucleotides in exon 10 of the CFTR gene in a Soviet family with cystic fibrosis causing early infant death

Author:

Ivaschenko Tatyana E.,White Marga Belle,Dean Michael,Baranov Vladislov S.

Publisher

Elsevier BV

Subject

Genetics

Reference8 articles.

1. Baranov V. S., Ivaschenko, T. E., Corbunova, V. N., Livshitz, L. A., Venozinskis, W. T., Gembovskaya, S. A., Kalinin, V. N., et al. Frequency of the ΔF508 deletion in cystic fibrosis patients from the European part of the USSR. Submitted for publication.

2. A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein;Cutting;Nature,1990

3. Worldwide survey of the ΔF508 mutation;Cystic Fibrosis Genetic Analysis Consortium;Am. J. Hum. Genet,1990

4. Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients;Dean;Cell,1990

5. Identification of the cystic fibrosis gene: Genetic analysis;Kerem;Science,1989

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