G970R‐CFTR Mutation (c.2908G>C) Results Predominantly in a Splicing Defect
In previous work, participants with a G970R mutation in cystic fibrosis transmembrane conductance regulator (CFTR) (c.2908G>C) had numerically lower sweat chloride responses during ivacaftor treatment than participants with other CFTR gating mutations. The objective of this substudy was to charac...
Main Authors: | , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Wiley
2021-03-01
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Series: | Clinical and Translational Science |
Online Access: | https://doi.org/10.1111/cts.12927 |