The clinical and molecular landscape of congenital myasthenic syndromes in Austria: a nationwide study

BACKGROUND: Congenital myasthenic syndromes (CMS) are a heterogeneous group of disorders caused by genetic defects resulting in impaired neuromuscular transmission. Although effective treatments are available, CMS is probably underdiagnosed, and systematic clinico-genetic investigations are warrante...

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Detalles Bibliográficos
Autores principales: Krenn, Martin, Sener, Merve, Rath, Jakob, Zulehner, Gudrun, Keritam, Omar, Wagner, Matias, Laccone, Franco, Iglseder, Stephan, Marte, Sonja, Baumgartner, Manuela, Eisenkölbl, Astrid, Liechtenstein, Christian, Rudnik, Sabine, Quasthoff, Stefan, Grinzinger, Susanne, Spenger, Johannes, Wortmann, Saskia B., Löscher, Wolfgang N., Zimprich, Fritz, Kellersmann, Anna, Rappold, Mika, Bernert, Günther, Freilinger, Michael, Cetin, Hakan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Original Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9886627/
https://www.ncbi.nlm.nih.gov/pubmed/36308527
http://dx.doi.org/10.1007/s00415-022-11440-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9886627/
https://www.ncbi.nlm.nih.gov/pubmed/36308527
http://dx.doi.org/10.1007/s00415-022-11440-0

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