Reduced penetrance of gene variants causing amyotrophic lateral sclerosis.

Douglas, Andrew G L; Baralle, Diana

Douglas, Andrew G L; Baralle, Diana.

Affiliation

Douglas AGL; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK andrew.douglas@ndcn.ox.ac.uk.
Baralle D; Human Development and Health, University of Southampton Faculty of Medicine, Southampton, UK.

J Med Genet ; 61(3): 294-297, 2024 Feb 21.

Article in En | MEDLINE | ID: mdl-38123999

Subject(s)

Amyotrophic Lateral Sclerosis; Frontotemporal Dementia; Humans; Amyotrophic Lateral Sclerosis/epidemiology; Amyotrophic Lateral Sclerosis/genetics; Amyotrophic Lateral Sclerosis/pathology; Frontotemporal Dementia/epidemiology; Frontotemporal Dementia/genetics; C9orf72 Protein/genetics; Penetrance; Superoxide Dismutase-1/genetics

Key words

Dementia; Genetic Predisposition to Disease; Genetics, Population; Motor Neuron Disease

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Full text: 1 Database: MEDLINE Main subject: Frontotemporal Dementia / Amyotrophic Lateral Sclerosis Limits: Humans Language: En Year: 2024 Type: Article

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Full text: 1 Database: MEDLINE Main subject: Frontotemporal Dementia / Amyotrophic Lateral Sclerosis Limits: Humans Language: En Year: 2024 Type: Article