Dysregulation of AMPA receptor subunit expression in sporadic ALS post‐mortem brain

Amyotrophic lateral sclerosis (ALS) is characterised by progressive motor neuron degeneration. Although there are over 40 genes associated with causal monogenetic mutations, the majority of ALS patients are not genetically determined. Causal ALS mutations are being increasingly mechanistically studi...

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Detalles Bibliográficos
Autores principales: Gregory, Jenna M, Livesey, Matthew R, McDade, Karina, Selvaraj, Bhuvaneish T, Barton, Samantha K, Chandran, Siddharthan, Smith, Colin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2019
Materias:
Original Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973025/
https://www.ncbi.nlm.nih.gov/pubmed/31579943
http://dx.doi.org/10.1002/path.5351

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973025/
https://www.ncbi.nlm.nih.gov/pubmed/31579943
http://dx.doi.org/10.1002/path.5351

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