Lack of full sequencing GBA1 studies for patients with Parkinson’s disease in Latin America
出版年份 2022 全文链接
标题
Lack of full sequencing GBA1 studies for patients with Parkinson’s disease in Latin America
作者
关键词
-
出版物
npj Parkinsons Disease
Volume 8, Issue 1, Pages -
出版商
Springer Science and Business Media LLC
发表日期
2022-08-08
DOI
10.1038/s41531-022-00358-z
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- 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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