Genetic testing in motor neurone disease
Share this article
Click the icon of the social media platform on which you would like to share this article.
Email this article to a friend
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Other content recommended for you
- Comprehensive analysis of the mutation spectrum in 301 German ALS families
- Value of systematic genetic screening of patients with amyotrophic lateral sclerosis
- Analysis of known amyotrophic lateral sclerosis and frontotemporal dementia genes reveals a substantial genetic burden in patients manifesting both diseases not carrying the C9orf72 expansion mutation
- Genetics insight into the amyotrophic lateral sclerosis/frontotemporal dementia spectrum
- CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis
- Pathophysiological insights into ALS with C9ORF72 expansions
- Genetic testing and reproductive choice in neurological disorders
- Neurofilament light chain in serum for the diagnosis of amyotrophic lateral sclerosis
- Effect of familial clustering in the genetic screening of 235 French ALS families
- FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis