Study of cognitive impairment and genetic polymorphism of SLC41A1 (rs11240569 allele) in Parkinson’s disease in Upper Egypt: case-control study

Study of cognitive impairment and genetic polymorphism of SLC41A1 (rs11240569 allele) in Parkinson’s disease in Upper Egypt: case-control study

Abstract Background Parkinson’s disease is one of the neurodegenerative disorders that is caused by genetic and environmental factors or interaction between them. Solute carrier family 41 member 1 within the PARK16 locus has been reported to be associated with Parkinson’s disease. Cognitive impairme...

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Bibliographic Details
Main Authors: Hamdy N. El-Tallawy, Tahia H. Saleem, Wafaa M. Farghaly, Heba Mohamed Saad Eldien, Ashraf Khodaery, Sherif A. Sayed, Ahmed A. Helaly, Hassan Mohammed Elnady
Format: Article
Language:English
Published: SpringerOpen 2021-06-01
Series:The Egyptian Journal of Neurology, Psychiatry and Neurosurgery
Subjects:
Parkinson’s disease
SLC41A1
rs11240569
Dementia
Cognitive Impairment
Online Access:https://doi.org/10.1186/s41983-021-00341-0

Internet

https://doi.org/10.1186/s41983-021-00341-0

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