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On the mechanism of gating defects caused by the R117H mutation in cystic fibrosis transmembrane conductance regulator

KEY POINTS: Two functional abnormalities of cystic fibrosis transmembrane conductance regulator (CFTR), a 25% reduction of the single‐channel conductance (g) and a ∼13‐fold lower open probability (P (o)), were found with the R117H mutation that is associated with mild forms of cystic fibrosis. Chara...

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Библиографические подробности
Опубликовано в: :J Physiol
Главные авторы: Yu, Ying‐Chun, Sohma, Yoshiro, Hwang, Tzyh‐Chang
Формат: Artigo
Язык:Inglês
Опубликовано: John Wiley and Sons Inc. 2016
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4908022/
https://ncbi.nlm.nih.gov/pubmed/26846474
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/JP271723
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