Muscular Dystrophy Research Today is a free monthly online journal that collates and summarizes the latest research about Muscular Dystrophy, including details on duchenne muscular dystrophy, symptoms, treatment.

Volume 3 (2007), Issue 10 (October)

1. Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2A.
   J Med Genet, 44(10): 609-14. [Abstract] [Full-text]
2. Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy.
   Am J Hum Genet, 81(5): 884-94. [Abstract] [Full-text]
3. POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes.
   Biochem Biophys Res Commun, 363(4): 1033-7. [Abstract] [Full-text]
4. A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy.
   Hum Mol Genet, 16(22): 2669-82. [Abstract] [Full-text]
5. VEGF overexpression via adeno-associated virus gene transfer promotes skeletal muscle regeneration and enhances muscle function in mdx mice.
   FASEB J, 21(13): 3737-46. [Abstract] [Full-text]

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