Case report: Three adult brothers with cystic fibrosis (delF508-delF508) maintain unusually preserved clinical profile in the absence of standard CF care

Author:

Bishop Clark T.

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine

Reference39 articles.

1. Cystic Fibrosis Foundation (n.d.) “What is Cystic Fibrosis?,” https://www.cff.org/What-is-CF/About-Cystic-Fibrosis/, accessed 25 September 2020.

2. Average Life Expectancies for Cystic Fibrosis;Leonard,2019

3. Preserving lung function: the holy grail in managing cystic fibrosis;Sly;Ann. Am.Thorac. Soc.,2017

4. Cystic Fibrosis Foundation (n.d.) “Types of CFTR Mutations,” https://www.cff.org/What-is-CF/Genetics/Types-of-CFTR-Mutations/, accessed 20 September 2020.

5. The DelF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigs;Ostedgaard;Sci. Transl. Med.,2011

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