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Dedicated research for a cure for cystic fibrosis.

Promoting independent research to ameliorate cystic fibrosis

The most frequently occurring mutation, delta-F508, is a single amino acid deletion in exon 10 which codes for a portion of the first nucleotide binding function (NBF-1) domain of the cystic fibrosis transmembrane conductance regulation protein. A list of other CF mutations is available.

Information resource for the Aztreonam Lysinate for Inhalation Research in Cystic Fibrosis clinical trials.