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Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy
2007
431 citations
Journal Article
Field-Weighted Citation Impact:
8.20
Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy | Researchclopedia
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Royal Manchester Children's Hospital
Jean‐Marie Garnier
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Eurométropole de Strasbourg
Valérie Biancalana
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Laboratoire de Génétique Médicale
Anders Oldfors
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Sahlgrenska University Hospital
Jean‐Louis Mandel
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Université de Strasbourg
Jocelyn Laporte
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Université de Strasbourg