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Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2.
Calandra, Patrizia; Cascino, Isabella; Lemmers, Richard J L F; Galluzzi, Giuliana; Teveroni, Emanuela; Monforte, Mauro; Tasca, Giorgio; Ricci, Enzo; Moretti, Fabiola; van der Maarel, Silvère M; Deidda, Giancarlo.
Afiliação
  • Calandra P; Institute of Cell Biology and Neurobiology, National Research Council of Italy, Monterotondo (Rome), Italy.
  • Cascino I; Institute of Cell Biology and Neurobiology, National Research Council of Italy, Monterotondo (Rome), Italy.
  • Lemmers RJ; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Galluzzi G; Institute of Cell Biology and Neurobiology, National Research Council of Italy, Monterotondo (Rome), Italy.
  • Teveroni E; Institute of Cell Biology and Neurobiology, National Research Council of Italy, Monterotondo (Rome), Italy Institute of Pathology, Catholic University School of Medicine, Rome, Italy.
  • Monforte M; Institute of Neurology, Catholic University School of Medicine, Rome, Italy.
  • Tasca G; Don Carlo Gnocchi Onlus Foundation, Milan, Italy.
  • Ricci E; Institute of Neurology, Catholic University School of Medicine, Rome, Italy.
  • Moretti F; Institute of Cell Biology and Neurobiology, National Research Council of Italy, Monterotondo (Rome), Italy.
  • van der Maarel SM; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Deidda G; Institute of Cell Biology and Neurobiology, National Research Council of Italy, Monterotondo (Rome), Italy.
J Med Genet ; 53(5): 348-55, 2016 05.
Article em En | MEDLINE | ID: mdl-26831754
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 4 / Músculo Esquelético / Metilação de DNA / Distrofia Muscular Facioescapuloumeral / Alelos Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 4 / Músculo Esquelético / Metilação de DNA / Distrofia Muscular Facioescapuloumeral / Alelos Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article