Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registry

Facioscapulohumeral dystrophy (FSHD) is a rare inherited neuromuscular disease estimated to affect 1/15,000 people. Through basic research, remarkable progress has been made towards the development of targeted therapies. Patient identification, through registries or other means is essential for tria...

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Detalles Bibliográficos
Autores principales: Evangelista, Teresinha, Wood, Libby, Fernandez-Torron, Roberto, Williams, Maggie, Smith, Debbie, Lunt, Peter, Hudson, Judith, Norwood, Fiona, Orrell, Richard, Willis, Tracey, Hilton-Jones, David, Rafferty, Karen, Guglieri, Michela, Lochmüller, Hanns
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Original Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929161/
https://www.ncbi.nlm.nih.gov/pubmed/27159994
http://dx.doi.org/10.1007/s00415-016-8132-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929161/
https://www.ncbi.nlm.nih.gov/pubmed/27159994
http://dx.doi.org/10.1007/s00415-016-8132-1

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