UNC13A in amyotrophic lateral sclerosis: from genetic association to therapeutic target

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with limited treatment options and an incompletely understood pathophysiology. Although genomewide association studies (GWAS) have advanced our understanding of the disease, the precise manner in which risk polymorphisms contri...

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Detalles Bibliográficos
Autores principales: Willemse, Sean W, Harley, Peter, van Eijk, Ruben P A, Demaegd, Koen C, Zelina, Pavol, Pasterkamp, R Jeroen, van Damme, Philip, Ingre, Caroline, van Rheenen, Wouter, Veldink, Jan H, Kiernan, Matthew C, Al-Chalabi, Ammar, van den Berg, Leonard H, Fratta, Pietro, van Es, Michael A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Neurodegeneration
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10359588/
https://www.ncbi.nlm.nih.gov/pubmed/36737245
http://dx.doi.org/10.1136/jnnp-2022-330504

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10359588/
https://www.ncbi.nlm.nih.gov/pubmed/36737245
http://dx.doi.org/10.1136/jnnp-2022-330504

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