Phenotypic characterization of two unrelated UK families with X-linked myopathy and an identical mutation in the FHL1 gene (2008)

Author(s): Sarkozy A, Bushby K, Hilton-Jones D, Dougan CF, Lochmuller H, Windpassinger C, Straub V

      • Date: 29 September - 2 October 2008
      • Conference Name: Neuromuscular Disorders: 13th International Congress of the World Muscle Society
      • Volume: 18 (9-10)
      • Pages: 819
      • Publisher: Elsevier Ltd
      • Publication type: Conference Proceedings (inc. abstract)
      • Bibliographic status: Published



      Professor Hanns Lochmuller
      Professor of Experimental Myology