Comparing knowledge and attitudes towards genetic testing in Parkinson's disease in an American and Asian population
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference19 articles.
1. Genetic testing in Parkinson's disease: promises and pitfalls;Tan;Arch Neurol,2006
2. Mutations in LRRK2 cause autosomal-dominant Parkinsonism with pleomorphic pathology;Zimprich;Neuron,2004
3. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease;Paisan-Ruiz;Neuron,2004
4. LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews;Ozelius;N Engl J Med,2006
5. The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence;Tan;Hum Genet,2006
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1. Hope vs. Hype II: It is time to offer pre-symptomatic genetic testing for GBA and LRRK2 variants;Parkinsonism & Related Disorders;2024-09
2. Knowledge, Attitudes and Perceptions of Genetic Testing Among Patients With Movement Disorders, Their Caregivers and Health Care Professionals;Journal of Movement Disorders;2024-07-31
3. Genetic Testing of Movements Disorders: A Review of Clinical Utility;Tremor and Other Hyperkinetic Movements;2024
4. Genetic literacy and attitude towards genetic testing in patients with Parkinson's disease and their caregivers: A review of literature;Parkinsonism & Related Disorders;2023-12
5. Genetic Testing for Parkinson's Disease and Movement Disorders in Less Privileged Areas: Barriers and Opportunities;Movement Disorders Clinical Practice;2023-11-29
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