A Dutch family with autosomal recessively inherited lower motor neuron predominant motor neuron disease due to optineurin mutations
Author:
Publisher
Informa UK Limited
Subject
Neurology (clinical),Neurology
Link
http://www.tandfonline.com/doi/pdf/10.3109/21678421.2015.1066821
Reference5 articles.
1. State of play in amyotrophic lateral sclerosis genetics
2. Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis
3. Mutations of optineurin in amyotrophic lateral sclerosis
4. A novel heterozygous nonsense mutation of the OPTN gene segregating in a Danish family with ALS
5. Evidence for an oligogenic basis of amyotrophic lateral sclerosis
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