Associated Papers
Targeted next-generation sequencing identifies novel variants in candidate genes for Parkinson's disease in Black South African and Nigerian patients.
Oluwole OG et al.
Bmc Medical Genetics, 2020
32019516 (PubMed )
Supplement: 12881_2020_953_MOESM8_ESM.xlsx › Variants_identified_in_PD_genes
Mutation screening of PLA2G6 in Japanese patients with early onset dystonia-parkinsonism.
Yamashita C et al.
Journal of Neural Transmission (vienna, Austria : 1996), 2017
Parkinson's disease: from genetics to treatments.
Fan HC et al.
Cell Transplantation, 2013
Analysis of PLA2G6 gene mutation in sporadic early-onset parkinsonism patients from Chinese population.
Tian JY et al.
Neuroscience Letters, 2012
PLA2G6 mutations in PARK14-linked young-onset parkinsonism and sporadic Parkinson's disease.
Lu CS et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2012
PLA2G6 variant in Parkinson's disease.
Tomiyama H et al.
Journal of Human Genetics, 2011
Myostatin depletion: a therapy for Ehlers-Danlos syndrome?
Prontera P et al.
Annals of Neurology, 2010
Select a paper to view details