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217. Cystic fibrosis mutations report from the French patients registry

โœ Scribed by J. Feingold; M. Guilloud-Bataille; D. De Crozes


Book ID
117455067
Publisher
Elsevier Science
Year
1999
Tongue
English
Weight
15 KB
Volume
54
Category
Article
ISSN
0300-2977

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## Communicated by Jurgen Horst A 2 bp deletion in exon 10 of the CFTR gene, 1677delTA, which is very rare among CF chromosomes worldwide, was found to be a relatively common cause of cystic fibrosis in countries located in the region of the Black Sea. The frequency of the mutation was compared am