Changes in mTOR/4‐EBP1 pathway induced by a novel mutation in PRKAG2 gene (864.7)

Yanchun Xu,Yi‐Tang Tseng,James Padbury,Laura C. Kobashigawa,Chanika Phornphutkul,D. Grahame Hardie

The FASEB Journal（2014）

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摘要

Objective: The genetics of hypertrophic cardiomyopathy (HCM) is heterogeneous. Mutations in PRKAG2 have been implicated in some previous cases of HCM. PRKAG2 encodes the γ2 isoform of AMPK, a heter...

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