Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes

M. Fanin, A. C. Nascimbeni, S. Aurino, E. Tasca, E. Pegoraro, V. Nigro, C. Angelini
  • Neurology, April 2009, Wolters Kluwer Health
  • DOI: 10.1212/wnl.0b013e3181a1885e

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http://dx.doi.org/10.1212/wnl.0b013e3181a1885e

The following have contributed to this page: Prof Corrado Angelini