Three faces of the same gene: FA2H links neurodegeneration with brain iron accumulation, leukodystrophies, and hereditary spastic paraplegias
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference18 articles.
1. Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA);Kruer;Ann Neurol,2010
2. Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia;Edvardson;Am J Hum Genet,2008
3. Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35);Dick;Hum Mutat,2010
4. Complicated recessive dystonia parkinsonism syndromes;Schneider;Mov Disord,2009
5. Potential role of ceramide metabolism in Lewy body disease;Bras;Eur J Biochem,2008
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