Associated Papers
Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosis.
Ruf WP et al.
Brain Communications, 2023
37223130 (PubMed )
Supplement: fcad152_supplementary_data.pdf
The ATP Synthase Deficiency in Human Diseases.
Galber C et al.
Life (basel, Switzerland), 2021
RNAi: a potential new class of therapeutic for human genetic disease.
Seyhan AA
Human Genetics, 2011
Friedreich ataxia: molecular mechanisms, redox considerations, and therapeutic opportunities.
Santos R et al.
Antioxidants & Redox Signaling, 2010
Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 families.
Lesca G et al.
Neurology, 2003
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