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Absence of alsin function leads to corticospinal motor neuron vulnerability via novel disease mechanisms

Mutations in the ALS2 gene result in early-onset amyotrophic lateral sclerosis, infantile-onset ascending hereditary spastic paraplegia and juvenile primary lateral sclerosis, suggesting prominent upper motor neuron involvement. However, the importance of alsin function for corticospinal motor neuro...

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Dades bibliogràfiques
Publicat a:Hum Mol Genet
Autors principals: Gautam, Mukesh, Jara, Javier H., Sekerkova, Gabriella, Yasvoina, Marina V., Martina, Marco, Özdinler, P. Hande
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2016
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4764190/
https://ncbi.nlm.nih.gov/pubmed/26755825
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv631
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