Pages that link to "Q48232175"
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The following pages link to SNCA variants rs2736990 and rs356220 as risk factors for Parkinson's disease but not for amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population (Q48232175):
Displaying 9 items.
- Genetics Underlying Atypical Parkinsonism and Related Neurodegenerative Disorders (Q26779001) (← links)
- Variants in SNCA Gene Are Associated with Parkinson's Disease Risk and Cognitive Symptoms in a Brazilian Sample. (Q33813336) (← links)
- Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population (Q35712293) (← links)
- Multiple system atrophy: the application of genetics in understanding etiology (Q37566673) (← links)
- Genetic Variants in SNCA and the Risk of Sporadic Parkinson's Disease and Clinical Outcomes: A Review (Q38637878) (← links)
- Analysis and meta-analysis of five polymorphisms of the LINGO1 and LINGO2 genes in Parkinson's disease and multiple system atrophy in a Chinese population (Q40646499) (← links)
- SNCA Gene Polymorphism may Contribute to an Increased Risk of Alzheimer's Disease. (Q53377744) (← links)
- A Comprehensive Analysis of the Association Between Polymorphisms and the Risk of Parkinson's Disease (Q58556450) (← links)
- The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson's disease in Iranian population (Q87017078) (← links)