Cargando…
Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in SCN4A
Autores principales: | Elia, Nathaniel, Nault, Trystan, McMillan, Hugh J., Graham, Gail E., Huang, Lijia, Cannon, Stephen C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099287/ https://www.ncbi.nlm.nih.gov/pubmed/32265824 http://dx.doi.org/10.3389/fneur.2020.00181 |
Ejemplares similares
-
Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in SCN4A
por: Elia, Nathaniel, et al.
Publicado: (2020) -
Marathoning with myotonic dystrophy type 2 (proximal myotonic myopathy) and leukopenia
por: Finsterer, Josef, et al.
Publicado: (2017) -
2386. Examining Ways to Increase COVID-19 Vaccine Uptake through Motivational Interviewing
por: Reyes, Summer M, et al.
Publicado: (2023) -
SCN4A as modifier gene in patients with myotonic dystrophy type 2
por: Binda, Anna, et al.
Publicado: (2018) -
2386 Associations of transthoracic echocardiographic features with cardioembolic stroke among patients without atrial fibrillation
por: Johansen, Michelle C., et al.
Publicado: (2018)