Epidermolysis bullosa simplex with muscular dystrophy associated with PLEC deletion mutation

Valeria Carolina Alvarez1, Sini Tellervo Penttilä1, Valeria Luján Salutto1

  • 1Instituto de Investigaciones Médicas Dr. A. Lanari (V.C.A., V.L.S., C.G.M.), Buenos Aires, Argentina; Neuromuscular Research Center (S.T.P., B.U.), Tampere University and University Hospital, Folkhälsan Genetic Institute (B.U.), and Vasa Central Hospital (B.U.), Finland.

Neurology. Genetics
|October 22, 2016
PubMed

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