Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness

PURPOSE: Several hundred genetic muscle diseases have been described, all of which are rare. Their clinical and genetic heterogeneity means that a genetic diagnosis is challenging. We established an international consortium, MYO-SEQ, to aid the work-ups of muscle disease patients and to better under...

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Detalles Bibliográficos
Autores principales: Töpf, Ana, Johnson, Katherine, Bates, Adam, Phillips, Lauren, Chao, Katherine R., England, Eleina M., Laricchia, Kristen M., Mullen, Thomas, Valkanas, Elise, Xu, Liwen, Bertoli, Marta, Blain, Alison, Casasús, Ana B., Duff, Jennifer, Mroczek, Magdalena, Specht, Sabine, Lek, Monkol, Ensini, Monica, MacArthur, Daniel G., Straub, Volker
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462745/
https://www.ncbi.nlm.nih.gov/pubmed/32528171
http://dx.doi.org/10.1038/s41436-020-0840-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462745/
https://www.ncbi.nlm.nih.gov/pubmed/32528171
http://dx.doi.org/10.1038/s41436-020-0840-3

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