LAMA2loss-of-function mutation in a girl with a mild congenital muscular dystrophy

P. Prandini, A. Berardinelli, M. Fanin, F. Morello, E. Zardini, A. Pichiecchio, C. Uggetti, G. Lanzi, C. Angelini, E. Pegoraro
  • Neurology, September 2004, Wolters Kluwer Health
  • DOI: 10.1212/01.wnl.0000138498.66940.7f

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The following have contributed to this page: Prof Corrado Angelini