The UK Myotonic Dystrophy Patient Registry: facilitating and accelerating clinical research

Myotonic dystrophy type 1 (DM1) is the most frequent muscular dystrophy worldwide with complex, multi-systemic, and progressively worsening symptoms. There is currently no treatment for this inherited disorder and research can be challenging due to the rarity and variability of the disease. The UK M...

Descripción completa

Detalles Bibliográficos
Autores principales: Wood, Libby, Cordts, Isabell, Atalaia, Antonio, Marini-Bettolo, Chiara, Maddison, Paul, Phillips, Margaret, Roberts, Mark, Rogers, Mark, Hammans, Simon, Straub, Volker, Petty, Richard, Orrell, Richard, Monckton, Darren G., Nikolenko, Nikoletta, Jimenez-Moreno, Aura Cecilia, Thompson, Rachel, Hilton-Jones, David, Turner, Chris, Lochmüller, Hanns
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Original Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413526/
https://www.ncbi.nlm.nih.gov/pubmed/28397002
http://dx.doi.org/10.1007/s00415-017-8483-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413526/
https://www.ncbi.nlm.nih.gov/pubmed/28397002
http://dx.doi.org/10.1007/s00415-017-8483-2

Ejemplares similares