Cargando…
ATXN2 trinucleotide repeat length correlates with risk of ALS
We investigated a CAG trinucleotide repeat expansion in the ATXN2 gene in amyotrophic lateral sclerosis (ALS). Two new case-control studies, a British dataset of 1474 ALS cases and 567 controls, and a Dutch dataset of 1328 ALS cases and 691 controls were analyzed. In addition, to increase power, we...
Ejemplares similares
-
ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and
contribute to TDP-43 mislocalization
por: Tazelaar, Gijs H P, et al.
Publicado: (2020) -
The most prevalent genetic cause of ALS-FTD, C9orf72 synergizes the toxicity of ATXN2 intermediate polyglutamine repeats through the autophagy pathway
por: Ciura, Sorana, et al.
Publicado: (2016) -
The molecular basis of the frontotemporal lobar degeneration–amyotrophic lateral sclerosis spectrum
por: van Langenhove, Tim, et al.
Publicado: (2012) -
Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis
por: Gaastra, Benjamin, et al.
Publicado: (2016) -
PolyQ Repeat Expansions in ATXN2 Associated with ALS Are CAA Interrupted Repeats
por: Yu, Zhenming, et al.
Publicado: (2011)