α-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations

David J. Duggan, Marina Fanin, Elena Pegoraro, Corrado Angelini, Eric P. Hoffman
  • Journal of the Neurological Sciences, September 1996, Elsevier
  • DOI: 10.1016/0022-510x(96)00028-7

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http://dx.doi.org/10.1016/0022-510x(96)00028-7

The following have contributed to this page: Prof Corrado Angelini