Rapid Progression of Sporadic ALS in a Patient Carrying SOD1 p.Gly13Arg Mutation

Amyotrophic lateral sclerosis (ALS), the most common adult onset motor neuron disease, is pathologically characterized by progressive loss of the upper and lower motor neurons. Mutations in the Cu/Zn superoxide dismutase gene (SOD1) account for about 20% of familial ALS cases and a small percentage...

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Detalles Bibliográficos
Autores principales: Kim, Myung-Jin, Bae, Jae-Han, Kim, Jeong-Min, Kim, Hye Ryoun, Yoon, Byung-Nam, Sung, Jung-Joon, Ahn, Suk-Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Brain and Neural Science 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5195821/
https://www.ncbi.nlm.nih.gov/pubmed/28035186
http://dx.doi.org/10.5607/en.2016.25.6.347

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5195821/
https://www.ncbi.nlm.nih.gov/pubmed/28035186
http://dx.doi.org/10.5607/en.2016.25.6.347

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