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Pulmonary disease severity in men with ΔF508 cystic fibrosis and residual chloride secretion

✍ Scribed by Stephen R Thomas; Adam Jaffe; Duncan M Geddes; Margaret E Hodson; Eric WFW Alton


Book ID
117311385
Publisher
The Lancet
Year
1999
Tongue
English
Weight
105 KB
Volume
353
Category
Article
ISSN
0140-6736

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The majority of the identified cystic fibrosis (CF) mutations are very uncommon in the total patient population, making the correlation between the clinical presentation and the molecular alterations difficult. The largest deletion that has been described so far in C F is of 84 bp in exon 13, which