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Molecular temporal bone pathology: III. Genotyping of the ΔF508 deletion in the DNA of patients with cystic fibrosis

✍ Scribed by Phillip A. Wackym; Marc M. Kerner; Wayne W. Grody


Book ID
114497400
Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
398 KB
Volume
108
Category
Article
ISSN
0023-852X

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Cystic fibrosis patients with mutation 1
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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