Associated Papers
Substitution p.A350V in Na⁺/Mg²⁺ exchanger SLC41A1, potentially associated with Parkinson's disease, is a gain-of-function mutation.
Kolisek M et al.
Plos One, 2013
Solute Carrier Family SLC41, what do we really know about it?
Fleig A et al.
Wiley Interdisciplinary Reviews. Membrane Transport and Signaling, 2013
Genetic variants in the RAB7L1 and SLC41A1 genes of the PARK16 locus in Chinese Parkinson's disease patients.
Yan Y et al.
The International Journal of Neuroscience, 2011
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