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 journalArticle

6 Citations (Scopus)
Original languageEnglish
Pages (from-to)601-602
Number of pages2
JournalClinical Genetics
Volume82
Issue number6
DOIs
Publication statusPublished - Dec 2012

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Fanin, M., Benedicenti, F., Fritegotto, C., Nascimbeni, A. C., Peterle, E., Stanzial, F., ... Angelini, C. (2012). An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the Alps. Clinical Genetics, 82(6), 601-602. https://doi.org/10.1111/j.1399-0004.2012.01873.x

An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the Alps. / Fanin, M.; Benedicenti, F.; Fritegotto, C.; Nascimbeni, A. C.; Peterle, E.; Stanzial, F.; Cristofoletti, A.; Castellan, C.; Angelini, C.

In: Clinical Genetics, Vol. 82, No. 6, 12.2012, p. 601-602.

Research output: Contribution to journalArticle

Fanin, M, Benedicenti, F, Fritegotto, C, Nascimbeni, AC, Peterle, E, Stanzial, F, Cristofoletti, A, Castellan, C & Angelini, C 2012, 'An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the Alps', Clinical Genetics, vol. 82, no. 6, pp. 601-602. https://doi.org/10.1111/j.1399-0004.2012.01873.x
Fanin, M. ; Benedicenti, F. ; Fritegotto, C. ; Nascimbeni, A. C. ; Peterle, E. ; Stanzial, F. ; Cristofoletti, A. ; Castellan, C. ; Angelini, C. / An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the Alps. In: Clinical Genetics. 2012 ; Vol. 82, No. 6. pp. 601-602.
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