Article ID Journal Published Year Pages File Type
10745260 Parkinsonism & Related Disorders 2014 4 Pages PDF
Abstract
This study has shown loss of Mg2+ efflux function consequent to SLC41A1 R244H variant and SLC41A1 coding variants seem to be rare in Taiwanese PD.
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Ageing
Authors
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