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neuroscientist
Alan Renton
British neuroscientist (born 1976)
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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
State of play in amyotrophic lateral sclerosis genetics
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
PINK1 cleavage at position A103 by the mitochondrial protease PARL.
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.
Mitochondrial dysfunction triggered by loss of HtrA2 results in the activation of a brain-specific transcriptional stress response
Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy