Genetic testing in motor neurone disease.

Dharmadasa, Thanuja; Scaber, Jakub; Edmond, Evan; Marsden, Rachael; Thompson, Alexander; Talbot, Kevin; Turner, Martin R

Dharmadasa, Thanuja; Scaber, Jakub; Edmond, Evan; Marsden, Rachael; Thompson, Alexander; Talbot, Kevin; Turner, Martin R.

Affiliation

Dharmadasa T; Nuffield Department of Clinical Neurosciences, Oxford University, Oxford, UK.
Scaber J; Nuffield Department of Clinical Neurosciences, Oxford University, Oxford, UK.
Edmond E; Nuffield Department of Clinical Neurosciences, Oxford University, Oxford, UK.
Marsden R; Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Thompson A; Nuffield Department of Clinical Neurosciences, Oxford University, Oxford, UK.
Talbot K; Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Turner MR; Nuffield Department of Clinical Neurosciences, Oxford University, Oxford, UK.

Pract Neurol ; 22(2): 107-116, 2022 Apr.

Article de En | MEDLINE | ID: mdl-35027459

Sujet(s)
Mots clés

ALS; clinical neurology; genetics; motor neurone disease; neurogenetics

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Expansion de séquence répétée de l'ADN / Démence frontotemporale Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Humans Langue: En Journal: Pract Neurol Année: 2022 Type de document: Article Pays d'affiliation: Royaume-Uni

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