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Journal of Personalized Medicine|April 30, 2021

Phenotyping Rare CFTR Mutations Reveal Functional Expression Defects Restored by TRIKAFTATMOnofrio Laselva, Maria C Ardelean, Christine E Bear

FEBS Letters|October 28, 2020

Strategies for cystic fibrosis transmembrane conductance regulator inhibition: from molecular mechanisms to treatment for secretory diarrhoeasHugo R de Jonge, Maria C Ardelean, Marcel J C Bijvelds, et al.

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Showing results (1-10 of 2) with videos related to

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Journal of Personalized Medicine|April 30, 2021

Phenotyping Rare CFTR Mutations Reveal Functional Expression Defects Restored by TRIKAFTATMOnofrio Laselva, Maria C Ardelean, Christine E Bear

FEBS Letters|October 28, 2020

Strategies for cystic fibrosis transmembrane conductance regulator inhibition: from molecular mechanisms to treatment for secretory diarrhoeasHugo R de Jonge, Maria C Ardelean, Marcel J C Bijvelds, et al.

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