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[Mutations in amphiphysin 2 (BIN1) cause autosomal recessive centronuclear myopathy.]

Résumé : NOUVELLE : Mutations de l'amphiphysine 2 (BIN1) dans les myopathies centronucléaires récessives
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https://www.hal.inserm.fr/inserm-00203227
Contributor : Jocelyn Laporte <>
Submitted on : Friday, June 13, 2008 - 11:30:16 AM
Last modification on : Wednesday, September 23, 2020 - 4:33:27 AM
Long-term archiving on: : Thursday, September 27, 2012 - 2:00:24 PM

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  • HAL Id : inserm-00203227, version 1
  • PUBMED : 18154705

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Anne Toussaint, Anne-Sophie Nicot, Jean-Louis Mandel, Jocelyn Laporte. [Mutations in amphiphysin 2 (BIN1) cause autosomal recessive centronuclear myopathy.]. médecine/sciences, EDP Sciences, 2007, 23 (12), pp.1080-1082. ⟨inserm-00203227⟩

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