Clinical and Molecular Aspects of Senataxin Mutations in Amyotrophic Lateral Sclerosis 4-Reference-Cited by-同舟云学术

Clinical and Molecular Aspects of Senataxin Mutations in Amyotrophic Lateral Sclerosis 4

Published:2020-01-28 Issue:4 Volume:87 Page:547-555
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol

Author:

Grunseich Christopher¹^ORCID,Patankar Aneesh¹,Amaya Joshua¹,Watts Jason A.²,Li Dongjun³⁴,Ramirez Prisila³,Schindler Alice B.¹,Fischbeck Kenneth H.¹,Cheung Vivian G.³⁴⁵

Affiliation:

1. Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health Bethesda MD

2. Department of Medicine University of Michigan Ann Arbor MI

3. Life Sciences Institute, University of Michigan Ann Arbor MI

4. Howard Hughes Medical Institute Chevy Chase MD

5. Department of Pediatrics University of Michigan Ann Arbor MI

Funder

National Institute of Neurological Disorders and Stroke

Howard Hughes Medical Institute

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.25681

Reference28 articles.

1. Genetics of Amyotrophic Lateral Sclerosis

2. TDP-43A315T mutation in familial motor neuron disease

3. Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

4. Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

5. DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)

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