Apps

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDknown for

State of play in amyotrophic lateral sclerosis geneticsknown for

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyknown for

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosisknown for

PINK1 cleavage at position A103 by the mitochondrial protease PARL.known for

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.known for

Mitochondrial dysfunction triggered by loss of HtrA2 results in the activation of a brain-specific transcriptional stress responseknown for

Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophyknown for

Alan Renton

Alan Renton