Genotype-phenotype association in patients with SCN4A mutation - Authors' reply.

Matthews, Emma; Männikkö, Roope; Behr, Elijah; Hanna, Michael G

Matthews, Emma; Männikkö, Roope; Behr, Elijah; Hanna, Michael G.

Afiliação

Matthews E; MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery, Queen Square, London, WC1N 3BG, UK. Electronic address: emma.matthews@ucl.ac.uk.
Männikkö R; MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery, Queen Square, London, WC1N 3BG, UK.
Behr E; Cardiology Clinical Academic Group, St George's University of London, London, UK; St George's University Hospitals NHS Foundation Trust, London, UK.
Hanna MG; MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery, Queen Square, London, WC1N 3BG, UK.

Lancet ; 393(10188): 2301-2302, 2019 06 08.

Article em En | MEDLINE | ID: mdl-31180027

Assuntos

Canal de Sódio Disparado por Voltagem NAV1.4/genética; Estudos de Associação Genética; Humanos; Mutação

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canal de Sódio Disparado por Voltagem NAV1.4 Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Lancet Ano de publicação: 2019 Tipo de documento: Article País de publicação: Reino Unido

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