Parkinsonism in complex neurogenetic disorders: lessons from hereditary dementias, adult-onset ataxias and spastic paraplegias.
Aloisio S, Satolli S, Bellini G, Lopriore P.
Neurol Sci. 2023 Oct;44(10):3379-3388. doi: 10.1007/s10072-023-07044-9. Epub 2023 Aug 30.
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Hereditary Parkinsonism-Associated Genetic Variations in PARK9 Locus Lead to Functional Impairment of ATPase Type 13A2.
Park JS, Sue CM.
Curr Protein Pept Sci. 2017;18(7):725-732. doi: 10.2174/1389203717666160311121534.
PMID:26965689
Frequency of Hereditary and GBA1-Related Parkinsonism in Latin America: A Systematic Review and Meta-Analysis.
Saffie Awad P, Teixeira-Dos-Santos D, Santos-Lobato BL, Camargos S, Cornejo-Olivas M, de Mello Rieder CR, Mata IF, Chaná-Cuevas P, Klein C, Schumacher Schuh AF.
Mov Disord. 2024 Jan;39(1):6-16. doi: 10.1002/mds.29614. Epub 2023 Nov 3.
PMID:37921246
The roles of PINK1, parkin, and mitochondrial fidelity in Parkinson's disease.
Pickrell AM, Youle RJ.
Neuron. 2015 Jan 21;85(2):257-73. doi: 10.1016/j.neuron.2014.12.007.
PMID:25611507
Hereditary Disorders of Manganese Metabolism: Pathophysiology of Childhood-Onset Dystonia-Parkinsonism in SLC39A14 Mutation Carriers and Genetic Animal Models.
Rodichkin AN, Guilarte TR.
Int J Mol Sci. 2022 Oct 24;23(21):12833. doi: 10.3390/ijms232112833.
PMID:36361624
New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.