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Genetic Testing for Parkinson's Disease and Movement Disorders in Less Privileged Areas: Barriers and Opportunities.

作者信息

Tan Ai Huey, Cornejo-Olivas Mario, Okubadejo Njideka, Pal Pramod Kumar, Saranza Gerard, Saffie-Awad Paula, Ahmad-Annuar Azlina, Schumacher-Schuh Artur F, Okeng'o Kigocha, Mata Ignacio F, Gatto Emilia M, Lim Shen-Yang

机构信息

Division of Neurology, Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

Neurogenetics Working Group, Universidad Científica del Sur, Lima, Peru.

出版信息

Mov Disord Clin Pract. 2024 Jan;11(1):14-20. doi: 10.1002/mdc3.13903. Epub 2023 Nov 29.

Abstract
摘要

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本文引用的文献

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Rev Med Chil. 2022 Nov;150(11):1547-1548. doi: 10.4067/S0034-98872022001101547.
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Genetic Movement Disorders Commonly Seen in Asians.
Mov Disord Clin Pract. 2023 May 8;10(6):878-895. doi: 10.1002/mdc3.13737. eCollection 2023 Jun.
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The lived experience of stigma and parkinson's disease in Kenya: a public health challenge.
BMC Public Health. 2023 Feb 20;23(1):364. doi: 10.1186/s12889-023-15278-7.
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Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort.
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MDSGene: Extending the List of Isolated Dystonia Genes by VPS16, EIF2AK2, and AOPEP.
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Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions.
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Six Action Steps to Address Global Disparities in Parkinson Disease: A World Health Organization Priority.
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Is there a way to reduce the inequity in variant interpretation on the basis of ancestry?
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Autosomal Recessive Cerebellar Ataxias in South America: A Multicenter Study of 1338 Patients.
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