Homozygous PLA2G6 (PARK 14) gene mutation associated neuropsychiatric phenotypes from southern India
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference4 articles.
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2. Exome sequencing in adult neurology practice: challenges and rewards in a mixed resource setting;Nagappa;Clin. Neurol. Neurosurg.,2018
3. Novel and reported variants in Parkinson's disease genes confer high disease burden among Indians;Kumar;Park. Relat. Disord.,2020
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1. Parkinson’s disease and schizophrenia interactomes contain temporally distinct gene clusters underlying comorbid mechanisms and unique disease processes;Schizophrenia;2024-02-27
2. The Clinical, Radiological and Genetic Spectrum of PLA2G6-Associated Neurodegeneration: An Experience From a Tertiary Center;Tremor and Other Hyperkinetic Movements;2024
3. Missense variants inPLA2G6contribute to a spectrum of clinical syndromes and provide pharmacogenomic correlates;2023-04-06
4. Reply to: Juvenile PLA2G6 ‐parkinsonism due to Indian ‘Asian’ p.R741Q mutation, and response to STN DBS;Movement Disorders;2022-02-13
5. Unusual Presentation of PLA2G6 ‐Related Neurodegeneration with Retinal Vasculitis;Movement Disorders Clinical Practice;2021-11-18
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