Pathophysiological mechanisms of the autosomal dominant centronuclear myopathy due to Dynamin 2 mutations - Archive ouverte HAL
Communication Dans Un Congrès Année : 2022

Pathophysiological mechanisms of the autosomal dominant centronuclear myopathy due to Dynamin 2 mutations

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hal-03920027 , version 1 (03-01-2023)

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  • HAL Id : hal-03920027 , version 1

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Marc Bitoun. Pathophysiological mechanisms of the autosomal dominant centronuclear myopathy due to Dynamin 2 mutations. 17th International Congress on Neuromuscular Diseases, Jul 2022, Bruxels, Belgium. ⟨hal-03920027⟩
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