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Novel defects in collagen XII and VI expand the mixed myopathy/Ehlers-Danlos syndrome spectrum and lead to variant-specific alterations in the extracellular matrix.
Delbaere, Sarah; Dhooge, Tibbe; Syx, Delfien; Petit, Florence; Goemans, Nathalie; Destrée, Anne; Vanakker, Olivier; De Rycke, Riet; Symoens, Sofie; Malfait, Fransiska.
Afiliación
  • Delbaere S; Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Dhooge T; Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Syx D; Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Petit F; Department of Clinical Genetics, CHU Lille, Université Lille, Lille, France.
  • Goemans N; Department of Child Neurology, University Hospital Leuven, Leuven, Belgium.
  • Destrée A; Department of Development and Regeneration, University of Leuven, Leuven, Belgium.
  • Vanakker O; Center for Human Genetics, Institute of Pathology and Genetics, Gosselies, Belgium.
  • De Rycke R; Center for Medical Genetics, Department of Biomolecular Medicine, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Symoens S; Department of Biomedical Molecular Biology and Expertise Centre for Transmission Electron Microscopy, Ghent University, Ghent, Belgium.
  • Malfait F; Center for Inflammation Research and BioImaging Core, VIB, Ghent, Belgium.
Genet Med ; 22(1): 112-123, 2020 01.
Article en En | MEDLINE | ID: mdl-31273343

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Colágeno Tipo VI / Colágeno Tipo XII / Síndrome de Ehlers-Danlos / Secuenciación de Nucleótidos de Alto Rendimiento / Enfermedades Musculares / Mutación Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Colágeno Tipo VI / Colágeno Tipo XII / Síndrome de Ehlers-Danlos / Secuenciación de Nucleótidos de Alto Rendimiento / Enfermedades Musculares / Mutación Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Estados Unidos