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Recent advances in myotonic dystrophy type 2.
Ulane, Christina M; Teed, Sarah; Sampson, Jacinda.
Afiliação
  • Ulane CM; Department of Neurology, The Neurological Institute, Columbia University Medical Center, 710 West 168 St., New York, NY, 10032, USA, cu2119@mail.cumc.columbia.edu.
Curr Neurol Neurosci Rep ; 14(2): 429, 2014 Feb.
Article em En | MEDLINE | ID: mdl-24435591
Myotonic dystrophy is the commonest adult muscular dystrophy. Myotonic dystrophy type 1 (DM1) and myotonic dystrophy type 2 (DM2) are often discussed jointly, and although they share many clinical and molecular features, differences do exist. Historically, more is known about DM1 than about DM2. The literature in the field of myotonic dystrophy is broad, with advances in our understanding of DM2. This article reviews recent developments in DM2 with respect to diagnosis, systemic features, and molecular mechanisms of the disease.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Miotônicos Tipo de estudo: Diagnostic_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Miotônicos Tipo de estudo: Diagnostic_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article