No GGGGCC-hexanucleotide repeat expansion inC9ORF72in parkinsonism patients in Sweden-Reference-Cited by-同舟云学术

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No GGGGCC-hexanucleotide repeat expansion inC9ORF72in parkinsonism patients in Sweden

Published:2012-09-17 Issue:1 Volume:14 Page:26-29
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

Akimoto Chizuru,Forsgren Lars,Linder Jan,Birve Anna,Backlund Irene,Andersson Jörgen,Nilsson Ann-Charloth,Alstermark Helena,Andersen Peter M.

Publisher

Informa UK Limited

Subject

Neurology (clinical),Neurology

Link

http://www.tandfonline.com/doi/pdf/10.3109/17482968.2012.725415

Reference22 articles.

1. Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS

2. A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

3. Aggregation of neurodegenerative disease in ALS kindreds

4. Parkinsonism and motor neuron diseases: Twenty-seven patients with diverse overlap syndromes

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1. Small striatal huntingtin inclusions in patients with motor neuron disease with reduced penetrance and intermediate HTT gene expansions;Human Molecular Genetics;2024-09-13

2. Meta-analysis of the association between C9orf72 repeats and neurodegeneration diseases;Journal of Neurogenetics;2024-01-02

3. C9orf72 genetic screening in amyotrophic lateral sclerosis patients from Serbia;Genetika;2023

4. C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population;Genetika;2022

5. Insights into disease mechanisms and potential therapeutics for C9orf72-related amyotrophic lateral sclerosis/frontotemporal dementia;Ageing Research Reviews;2020-12

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