A cause for childhood ataxia.
expert_opinion · Level V
Where this comes from
- Record sourced from PubMed, PMID 26929993.
- Also identified by DOI 10.7554/eLife.14523 and PMC identifier 4786425.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Genetic studies uncover a mutation in a widely conserved protein as the cause of a neurological disorder in two brothers.
Medical subject headings
- Ataxia
- Mutation