The alpha2-subunit of the AP2 clathrin adaptor as the causal gene in an atypical myopathy with granulofilamentous inclusions - Archive ouverte HAL Accéder directement au contenu
Poster De Conférence Année : 2021

The alpha2-subunit of the AP2 clathrin adaptor as the causal gene in an atypical myopathy with granulofilamentous inclusions

G. Brochier
  • Fonction : Auteur
M. Fardeau
  • Fonction : Auteur
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hal-03983816 , version 1 (11-02-2023)

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G. Moulay, I. Nelson, J. Lainé, E. Cohen, M. Lemaître, et al.. The alpha2-subunit of the AP2 clathrin adaptor as the causal gene in an atypical myopathy with granulofilamentous inclusions. 26th International Congress of the World Muscle Society (WMS), Sep 2021, Virtual conference, United Kingdom. Neuromuscular Disorders, 31, pp.S141-S142, 2021, ⟨10.1016/j.nmd.2021.07.326⟩. ⟨hal-03983816⟩
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