Lack of full sequencing GBA1 studies for patients with Parkinson’s disease in Latin America
Published 2022 View Full Article
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Title
Lack of full sequencing GBA1 studies for patients with Parkinson’s disease in Latin America
Authors
Keywords
-
Journal
npj Parkinsons Disease
Volume 8, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2022-08-08
DOI
10.1038/s41531-022-00358-z
References
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Related references
Note: Only part of the references are listed.- Clinical and Genetic Analysis of Costa Rican Patients With Parkinson's Disease
- (2021) Gabriel Torrealba-Acosta et al. Frontiers in Neurology
- Next-Generation Sequencing Analysis of GBA1: The Challenge of Detecting Complex Recombinant Alleles
- (2021) Elizabeth G. Woo et al. Frontiers in Genetics
- Prevalence of GBA p.K198E mutation in Colombian and Hispanic populations
- (2020) Philip W. Tipton et al. PARKINSONISM & RELATED DISORDERS
- A Large‐Scale Full GBA1 Gene Screening in Parkinson's Disease in the Netherlands.
- (2020) Jonas M. Heijer et al. MOVEMENT DISORDERS
- Evaluation of the detection of GBA missense mutations and other variants using the Oxford Nanopore MinION
- (2019) Melissa Leija-Salazar et al. Molecular Genetics & Genomic Medicine
- The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru
- (2019) Carlos Velez-Pardo et al. PARKINSONISM & RELATED DISORDERS
- GBA mutations p.N370S and p.L444P are associated with Parkinson's disease in patients from Northern Brazil
- (2019) Carlos Eduardo de Melo Amaral et al. ARQUIVOS DE NEURO-PSIQUIATRIA
- Autosomal dominant Parkinson’s disease: Incidence of mutations in LRRK2, SNCA, VPS35 and GBA genes in Brazil
- (2016) Gabriella de M. Abreu et al. NEUROSCIENCE LETTERS
- Differential effects of severe vs mild GBA mutations on Parkinson disease
- (2015) Z. Gan-Or et al. NEUROLOGY
- Genetic Movement Disorders in Patients of Jewish Ancestry
- (2014) Rivka Inzelberg et al. JAMA Neurology
- The L444PGBAmutation is associated with early-onset Parkinson's disease in Mexican Mestizos
- (2013) M de L González-del Rincón et al. CLINICAL GENETICS
- Glucocerebrosidase N370S and L444P mutations as risk factors for Parkinson’s disease in Brazilian patients
- (2011) Beatriz de Carvalho Guimarães et al. PARKINSONISM & RELATED DISORDERS
- Mutational analysis of GIGYF2, ATP13A2 and GBA genes in Brazilian patients with early-onset Parkinson's disease
- (2010) Adriana Vaz dos Santos et al. NEUROSCIENCE LETTERS
- Parkinson's disease and the heterozygous state for glucocerebrosidase mutations among Brazilians
- (2008) Mariana P. Socal et al. PARKINSONISM & RELATED DISORDERS
- Association between Parkinson's disease and glucocerebrosidase mutations in Brazil
- (2007) Mariana Spitz et al. PARKINSONISM & RELATED DISORDERS
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