Cargando…
A clinical and genetic study of early‐onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next‐generation sequencing
BACKGROUND: Recent genetic progress has allowed for the molecular diagnosis of Parkinson's disease. However, genetic causes of PD vary widely in different ethnicities. Mutational frequencies and clinical phenotypes of genes associated with PD in Asian populations are largely unknown. The object...
Autores principales: | Lin, Chin‐Hsien, Chen, Pei‐Lung, Tai, Chun‐Hwei, Lin, Hang‐I, Chen, Chih‐Shan, Chen, Meng‐Ling, Wu, Ruey‐Meei |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594087/ https://www.ncbi.nlm.nih.gov/pubmed/30788857 http://dx.doi.org/10.1002/mds.27633 |
Ejemplares similares
-
The impact of nonmotor symptoms on quality of life in patients with Parkinson’s disease in Taiwan
por: Liu, Weng-Ming, et al.
Publicado: (2015) -
Mutational Analysis of Angiogenin Gene in Parkinson's Disease
por: Chen, Meng-Ling, et al.
Publicado: (2014) -
Novel variant Pro143Ala in HTRA2 contributes to Parkinson’s disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria
por: Lin, Chin-Hsien, et al.
Publicado: (2011) -
Plasma extracellular vesicle tau, β-amyloid, and α-synuclein and the
progression of Parkinson’s disease: a follow-up study
por: Chan, Lung, et al.
Publicado: (2023) -
National Trends of Antiparkinsonism Treatment in Taiwan: 2004–2011
por: Liu, Weng-Ming, et al.
Publicado: (2016)