Regulation of Intracellular Manganese Homeostasis by Kufor-Rakeb Syndrome-associated ATP13A2 Protein
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference53 articles.
1. Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
2. Clinical spectrum of Kufor-Rakeb syndrome in the Chilean kindred with ATP13A2 mutations
3. ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease
4. ATP13A2 variants in early-onset Parkinson's disease patients and controls
5. Clinical heterogeneity of ATP13A2 linked disease (Kufor-Rakeb) justifies a PARK designation
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