Should we monitor exhaled NO to assess the restoration of CFTR function in CF patients?
J Cyst Fibros
.
2015 Nov;14(6):683-4.
doi: 10.1016/S1569-1993(15)00247-7.
Authors
Anh T Dinh-Xuan
,
Thông Hua-Huy
PMID:
26566815
DOI:
10.1016/S1569-1993(15)00247-7
No abstract available
Publication types
Editorial
Comment
MeSH terms
Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
Cystic Fibrosis*
Exhalation
Humans
Mutation
Substances
Cystic Fibrosis Transmembrane Conductance Regulator