INNOVATIVE TREATMENTS FOR CYSTIC FIBROSIS


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Abstract

The review presents current etiological and pathogenetic methods for the personalized therapy of cystic fibrosis in relation to the class and type of mutation in the CFTR gene. It considers the first innovation agents for the treatment of cystic fibrosis and new promising developments.

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About the authors

Yu. Kondratyeva

Research Center for Medical Genetics, Moscow

Email: elenafpk@mail.ru
Professor, MD

References

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