Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.
Hsu SC; Sears RL; Lemos RR; Quintáns B; Huang A; Spiteri E; Nevarez L; Mamah C; Zatz M; Pierce KD; Fullerton JM; Adair JC; Berner JE; Bower M; Brodaty H; Carmona O; Dobricić V; Fogel BL; García-Estevez D; Goldman J; Goudreau JL; Hopfer S; Janković M; Jaumà S; Jen JC; Kirdlarp S; Klepper J; Kostić V; Lang AE; Linglart A; Maisenbacher MK; Manyam BV; Mazzoni P; Miedzybrodzka Z; Mitarnun W; Mitchell PB; Mueller J; Novaković I; Paucar M; Paulson H; Simpson SA; Svenningsson P; Tuite P; Vitek J; Wetchaphanphesat S; Williams C; Yang M; Schofield PR; de Oliveira JR; Sobrido MJ; Geschwind DH; Coppola G; Neurogenetics, 2013, vol. 14, issue 1, p 11, ISSN 13646753. ISBN 13646753.

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