The α2-subunit of the AP2 clathrin adaptor as a new causal gene in an atypical myopathy with granulofilamentous inclusions - CNRS - Centre national de la recherche scientifique Accéder directement au contenu
Poster De Conférence Année : 2021

The α2-subunit of the AP2 clathrin adaptor as a new causal gene in an atypical myopathy with granulofilamentous inclusions

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hal-03967904 , version 1 (01-02-2023)

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  • HAL Id : hal-03967904 , version 1

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Gilles Moulay, Isabelle Nelson, Jeanne Lainé, Enzo Cohen, Mégane Lemaître, et al.. The α2-subunit of the AP2 clathrin adaptor as a new causal gene in an atypical myopathy with granulofilamentous inclusions. Congress of the World Muscle Society, Sep 2021, Virtual, France. 2021. ⟨hal-03967904⟩
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