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Mutation-specific effects on thin filament length in thin filament myopathy.
Winter, Josine M de; Joureau, Barbara; Lee, Eun-Jeong; Kiss, Balázs; Yuen, Michaela; Gupta, Vandana A; Pappas, Christopher T; Gregorio, Carol C; Stienen, Ger J M; Edvardson, Simon; Wallgren-Pettersson, Carina; Lehtokari, Vilma-Lotta; Pelin, Katarina; Malfatti, Edoardo; Romero, Norma B; Engelen, Baziel G van; Voermans, Nicol C; Donkervoort, Sandra; Bönnemann, C G; Clarke, Nigel F; Beggs, Alan H; Granzier, Henk; Ottenheijm, Coen A C.
Afiliação
  • Winter JM; Department of Physiology, VU University Medical Center, Amsterdam, the Netherlands.
  • Joureau B; Department of Physiology, VU University Medical Center, Amsterdam, the Netherlands.
  • Lee EJ; Department of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ.
  • Kiss B; Department of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ.
  • Yuen M; Institute for Neuroscience and Muscle Research, Children's Hospital at Westmead, Westmead, New South Wales, Australia.
  • Gupta VA; Discipline of Paediatrics and Child Health, University of Sydney, Sydney, New South Wales, Australia.
  • Pappas CT; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, MA.
  • Gregorio CC; Department of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ.
  • Stienen GJ; Department of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ.
  • Edvardson S; Department of Physiology, VU University Medical Center, Amsterdam, the Netherlands.
  • Wallgren-Pettersson C; Department of Physics and Astronomy, VU University, Amsterdam, the Netherlands.
  • Lehtokari VL; Pediatric Neurology Unit, Hadassah University Hospital, Jerusalem, Israel.
  • Pelin K; Department of Medical and Clinical Genetics, Haartman Institute, University of Helsinki, Helsinki, Finland.
  • Malfatti E; Folkhaelsan Institute of Genetics, Biomedicum Helsinki, Helsinki, Finland.
  • Romero NB; Department of Medical and Clinical Genetics, Haartman Institute, University of Helsinki, Helsinki, Finland.
  • Engelen BG; Folkhaelsan Institute of Genetics, Biomedicum Helsinki, Helsinki, Finland.
  • Voermans NC; Folkhaelsan Institute of Genetics, Biomedicum Helsinki, Helsinki, Finland.
  • Donkervoort S; Division of Genetics, Department of Biosciences, University of Helsinki, Helsinki, Finland.
  • Bönnemann CG; Center for Research in Myology, Pitié-Salpêtrière Hospital Group, Paris, France.
  • Clarke NF; Center for Research in Myology, Pitié-Salpêtrière Hospital Group, Paris, France.
  • Beggs AH; Department of Neurology, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Granzier H; Department of Neurology, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Ottenheijm CA; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institutes of Health, Bethesda, MD.
Ann Neurol ; 79(6): 959-69, 2016 06.
Article em En | MEDLINE | ID: mdl-27074222
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcômeros / Citoesqueleto / Proteínas Musculares / Doenças Musculares Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: Ann Neurol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcômeros / Citoesqueleto / Proteínas Musculares / Doenças Musculares Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: Ann Neurol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda