Recurrent BAG3 gene mutation in a British family with two siblings with severe myofibrillar myopathy (2010)

Author(s): Sarkozy A, McKenna C, Straub V, Lochmuller H, Goldfarb LG, Bushby K

      • Date: 25-26 March 2010
      • Conference Name: Neuromuscular Disorders: United Kingdom Neuromuscular Translational Research Conference
      • Volume: 20 (s1)
      • Pages: S28
      • Publisher: Elsevier Ltd
      • Publication type: Conference Proceedings (inc. abstract)
      • Bibliographic status: Published



      Professor Katherine Bushby
      Act. Res.Chair of Neuromuscular Genetics

      Professor Hanns Lochmuller
      Professor of Experimental Myology

      Professor Volker Straub
      Harold Macmillan Professor of Medicine