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MYH7 gene mutation in myosin storage myopathy and scapulo-peroneal myopathy

  • Published:2007-04 Issue:4 Volume:17 Page:321-329
  • ISSN:0960-8966
  • Container-title:Neuromuscular Disorders
  • language:en
  • Short-container-title:Neuromuscular Disorders

Author:

Pegoraro Elena,Gavassini Bruno F.,Borsato Carlo,Melacini Paola,Vianello Andrea,Stramare Roberto,Cenacchi Giovanna,Angelini Corrado

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference17 articles.

1. Hyaline body myopathy: case report;Barhon;Neuromuscul Disord,1994

2. Familial myopathy with probable lysis of myofibrils in type I fibers;Cancilla;Neurology,1971

3. Hyaline bodies in skeletal muscle of a patient with a mild chronic non-progressive congenital myopathy;Ceuterick;Clin Neuropathol,1983

4. Myosin storage myopathy associated with a heterozygous missense mutation in MYH7;Tajsharghi;Ann Neurol,2003

5. Autosomal dominant hyaline body myopathy. Clinical variability and pathological findings;Bohlega;Neurology,2003

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