An ex vivo model contributing to the diagnosis and evaluation of new drugs in cystic fibrosis
La fibrosi cistica (FC) è una malattia autosomica recessiva causata da mutazioni nel gene CFTR (Cystic Fibrosis Transmembrane conductance Regulator). Finora sono state descritte circa 2000 mutazioni, ma per la maggior parte di esse è difficile definirne leffetto senza complesse procedure in vi...
Main Authors: | A.M. Di Lullo, M. Scorza, F. Amato, M. Comegna, V. Raia, L. Maiuri, G. Ilardi, E. Cantone, G. Castaldo, M. Iengo |
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Format: | Article |
Language: | English |
Published: |
Pacini Editore Srl
2017-06-01
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Series: | Acta Otorhinolaryngologica Italica |
Online Access: | https://www.actaitalica.it/issues/2017/3-2017/06_DiLullo.pdf |
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