Recurrent K3E mutation in Cu/Zn superoxide dismutase gene associated with amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

Recurrent K3E mutation in Cu/Zn superoxide dismutase gene associated with amyotrophic lateral sclerosis

Published:2013-07-30 Issue:7-8 Volume:14 Page:608-614
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

Kuźma-Kozakiewicz Magdalena,Berdyński Mariusz,Morita Mitsuya,Takahashi Yuji,Kawata Akihiro,Kaida Ken-Ichi,Kaźmierczak Beata,Łusakowska Anna,Goto Jun,Tsuji Shoji,Żekanowski Cezary,Kwieciński Hubert

Publisher

Informa UK Limited

Subject

Neurology (clinical),Neurology

Link

http://www.tandfonline.com/doi/pdf/10.3109/21678421.2013.812119

Reference19 articles.

1. Clinical genetics of amyotrophic lateral sclerosis: what do we really know?

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

3. SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis

4. Amyotrophic lateral sclerosis associated with mutations in the CuZn superoxide dismutase gene

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