Motor neuron disease: The curious ways of ALS.
review · Level V
Where this comes from
- Record sourced from PubMed, PMID 18633404.
- Also identified by DOI 10.1038/454284a and PMC identifier 3625042.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
That mutations in the SOD1 enzyme underlie familial form of the motor neuron disease ALS is clear. But there seems to be more than one answer to the question of what are the consequences of such mutations.
Medical subject headings
- Amyotrophic Lateral Sclerosis