Personalised medicine for non-classic cystic fibrosis resulting from rare CFTR mutations-Reference-Cited by-同舟云学术

Personalised medicine for non-classic cystic fibrosis resulting from rare CFTR mutations

Published:2020-04-07 Issue:1 Volume:56 Page:2000062
ISSN:0903-1936
Container-title:European Respiratory Journal
language:en
Short-container-title:Eur Respir J

Author:

McCravy Matthew S.,Quinney Nancy L.,Cholon Deborah M.,Boyles Susan E.,Jensen Timothy J.,Aleksandrov Andrei A.,Donaldson Scott H.,Noone Peadar G.,Gentzsch Martina

Funder

Cystic Fibrosis Foundation

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

European Respiratory Society (ERS)

Subject

Pulmonary and Respiratory Medicine

Reference16 articles.

1. Physiological Basis of Cystic Fibrosis: A Historical Perspective

2. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA

3. Correlating cystic fibrosis transmembrane conductance regulator function with clinical features to inform precision treatment of cystic fibrosis;McCague;Am J Respir Crit Care Med,2019

4. A 76 year old female diagnosed with cystic fibrosis;O'Brien;Ir Med J,2014

5. Comparison of the clinical manifestations of cystic fibrosis in black and white patients

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