Rare Diseases: Genetics and Metabolism

MRGM Research aims to decipher the molecular mechanisms laying at the root of the physiopathology of rare diseases and make our findings worth for patients.

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COSTELLO SYNDROME

April 14, 2022April 14, 2022 / mrgm_fr

HRAS germline mutations impair LKB1/AMPK signaling and mitochondrial homeostasis in Costello syndrome models

https://sbm.u-bordeaux.fr/actualites/mise-en-lumiere-de-la-publication-hras-germline-mutations-impair-lkb1ampk-signaling-and-mitochondrial-homeostasis-costello-syndr

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