[1] Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotype.J Am Soc Nephrol. 2013 May;24(6):967-77.

[2] Substitution p.A350V in Na(+)/Mg(2)(+) exchanger SLC41A1, potentially associated with Parkinson's disease, is a gain-of-function mutation.PLoS One. 2013 Aug 15;8(8):e71096.