Association between GRIN2B polymorphism and Parkinson’s disease risk, age at onset, and progression in Southern China
Background and objectivesThe role of N-methyl-D-aspartate receptor 2B (GRIN2B) single nucleotide polymorphisms (SNPs) in influencing the risk and progression of Parkinson’s disease (PD) is still unclear. This study aimed to assess the impact of GRIN2B genotype status on PD susceptibility and symptom...
Saved in:
| Main Authors: | Can Cui, Hongxia Li, Yiwen Bao, Yingying Han, Hongxiang Yu, Huan Song, Bei Zhang |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2024-12-01
|
| Series: | Frontiers in Neurology |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fneur.2024.1459576/full |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Parkinson's disease and polymorphisms of the glutamatergic system genes GRIN2A, SLC1A2, and GRIK4
by: Yu. S. Mironova, et al.
Published: (2018-06-01) -
Association between GRIN2B DNA methylation and cognitive impairment: a cross-sectional study of patients with bipolar depression
by: Hao Yu, et al.
Published: (2025-05-01) -
GRIN1‐related epilepsy in a neonate with response to memantine and vigabatrin
by: Isabella Eiler, et al.
Published: (2024-12-01) -
Preliminary Study About A Significant and Treatable Cause of Epileptic Encephalopathy: GRIN2D Mutation
by: Nadide Cemre Randa, et al.
Published: (2021-08-01) -
Exome sequencing reveals a rare damaging variant in GRIN2C in familial late-onset Alzheimer's disease
by: Elisa Rubino, et al.
Published: (2025-01-01)