An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the Alps

M Fanin, F Benedicenti, C Fritegotto, AC Nascimbeni, E Peterle, F Stanzial, A Cristofoletti, C Castellan, C Angelini
  • Clinical Genetics, April 2012, Wiley
  • DOI: 10.1111/j.1399-0004.2012.01873.x

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http://dx.doi.org/10.1111/j.1399-0004.2012.01873.x

The following have contributed to this page: Dr Francesco Benedicenti and Prof Corrado Angelini