New mutations found by Next-Generation Sequencing screening of Spanish patients with Nemaline Myopathy

Nemaline Myopathy (NM) is a rare genetic disorder that encompasses a large spectrum of myopathies characterized by hypotonia and generalized muscle weakness. To date, mutations in thirteen different genes have been associated with NM. The most frequently responsible genes are NEB (50% of cases) and...

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Detalles Bibliográficos
Autores principales: Moreau-Le Lan, Sarah, Aller, Elena, Calabria, Ines, Gonzalez-Tarancon, Lola, Cardona-Gay, Cristina, Martinez-Matilla, Marina, Aparisi, Maria J., Selles, Jorge, Sagath, Lydia, Pitarch, Inmaculada, Muelas, Nuria, Cervera, Jose V., Millan, Jose M., Pedrola, Laia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281284/
https://www.ncbi.nlm.nih.gov/pubmed/30517146
http://dx.doi.org/10.1371/journal.pone.0207296

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6281284/
https://www.ncbi.nlm.nih.gov/pubmed/30517146
http://dx.doi.org/10.1371/journal.pone.0207296

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