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, A. C. Nascimbeni, E. Peterle, F. Stanzial, A. Cristofoletti, C. Castellan, C. Angelini

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)601-602
Number of pages2
JournalClinical Genetics
Issue number6
Publication statusPublished - Dec 2012

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

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