Characterization of the amyotrophic lateral sclerosis-linked P56S mutation of the VAPB gene in Southern Brazil-Reference-Cited by-同舟云学术

Characterization of the amyotrophic lateral sclerosis-linked P56S mutation of the VAPB gene in Southern Brazil

Published:2020-03-12 Issue:3-4 Volume:21 Page:286-290
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

Trilico Matheus Luis Castelan¹^ORCID,Lorenzoni Paulo José²,Kay Cláudia Suemi Kamoi²,Ducci Renata Dal Pra²,Fustes Otto Jesus Hernandez²,Werneck Lineu Cesar²,Scola Rosana Herminia²

Affiliation:

1. Service of Neuromuscular Disorders, Division of Neurology, Department of Internal Medicine, Hospital de Clínicas, Universidade Federal do Paraná (UFPR), Curitiba, Brazil, and

2. Service of Neuromuscular Disorders, Division of Neurology, Department of Internal Medicine, Hospital de Clínicas, Universidade Federal do Paraná (UFPR), Curitiba, Brazil

Publisher

Informa UK Limited

Subject

Clinical Neurology,Neurology

Link

https://www.tandfonline.com/doi/pdf/10.1080/21678421.2020.1738495

Reference23 articles.

1. Amyotrophic lateral sclerosis

2. Genetic heterogeneity of amyotrophic lateral sclerosis: Implications for clinical practice and research

3. A comprehensive review of amyotrophic lateral sclerosis

4. A Mutation in the Vesicle-Trafficking Protein VAPB Causes Late-Onset Spinal Muscular Atrophy and Amyotrophic Lateral Sclerosis

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