A novel AFG3L2 mutation close to AAA domain leads to aberrant OMA1 and OPA1 processing in a family with optic atrophy

Overview of attention for article published in Acta Neuropathologica Communications, June 2020

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RT @ingentium_ms: A novel AFG3L2 mutation close to AAA domain leads to aberrant OMA1 and OPA1 processing in a family with optic atrophy. ht…

A novel AFG3L2 mutation close to AAA domain leads to aberrant OMA1 and OPA1 processing in a family with optic atrophy. https://t.co/fAV1r6F6RK https://t.co/4LHXEeKbuA

New article: A novel AFG3L2 mutation close to AAA domain leads to aberrant OMA1 and OPA1 processing in a family with optic atrophy. https://t.co/JrXBVXU9q6 #MS #multiplesclerosis #neurology https://t.co/jTzzlk9yPX

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