Class 1 CF Mutations

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Class 1 CF Mutations

Since the discovery of the gene that causes Cystic Fibrosis, our knowledge of how mutations in this gene cause the varied pathophysiological manifestations of this disease has increased substantially. This knowledge has led to the possibility of new therapeutic approaches aimed at the basic defect. Class I mutations of CFTR include premature termination codons (PTCs) or stop codons. In the last...

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ژورنال

عنوان ژورنال: Frontiers in Pharmacology

سال: 2012

ISSN: 1663-9812

DOI: 10.3389/fphar.2012.00117