Co-occurrence of PRKN and SYNJ1 variants in Early-Onset Parkinson's disease-Reference-Cited by-同舟云学术

Co-occurrence of PRKN and SYNJ1 variants in Early-Onset Parkinson's disease

Published:2024-06-05 Issue:5 Volume:39 Page:915-928
ISSN:1573-7365
Container-title:Metabolic Brain Disease
language:en
Short-container-title:Metab Brain Dis

Author:

Cotrin Juliana Cordovil,Piergiorge Rafael Mina,Gonçalves Andressa Pereira,Pereira João Santos,Gerber Alexandra Lehmkuhl,de Campos Guimarães Ana Paula,de Vasconcelos Ana Tereza Ribeiro,Santos-Rebouças Cíntia Barros

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

INOVUERJ

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro

Centro de Produção da Universidade do Estado do Rio de Janeiro

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s11011-024-01362-3.pdf

Reference59 articles.

1. Alcalay RN, Caccappolo E, Mejia-Santana H, Tang MX, Rosado L, Orbe Reilly M et al (2014) Cognitive and motor function in long-duration PARKIN-associated Parkinson disease. JAMA Neurol 71(1):62–7. https://doi.org/10.1001/jamaneurol.2013.4498

2. Angelopoulou E, Paudel YN, Papageorgiou SG, Piperi C (2022) Environmental impact on the epigenetic mechanisms underlying Parkinson’s disease pathogenesis: a narrative review. Brain Sci 12(2):175. https://doi.org/10.3390/brainsci12020175

3. Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, Cherry JM, Davis AP, Dolinski K, Dwight SS, Eppig JT, Harris MA, Hill DP, Issel-Tarver L, Kasarskis A, Lewis S, Matese JC, Richardson JE, Ringwald M, Rubin GM, Sherlock G (2000) Gene ontology: tool for the unification of biology. The gene ontology consortium. Nat Genet 25(1):25–29. https://doi.org/10.1038/75556

4. Bastian M, Heymann S, Jacomy M (2009) Gephi: an open source software for exploring and manipulating networks. In: International AAAI Conference on Weblogs and Social Media 3(1):361–362. https://doi.org/10.1609/icwsm.v3i1.13937

5. Ben Romdhan S, Sakka S, Farhat N, Triki S,Dammak M, Mhiri C (2018) A Novel SYNJ1 Mutation in a Tunisian Family with Juvenile Parkinson’s Disease Associated with Epilepsy. J Mol Neurosci 66(2):273-278. https://doi.org/10.1007/s12031-018-1167-2