학술논문
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification
Document Type
Artikel
Author
Hsu, SC; Sears, RL; Lemos, RR; Quintans, 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; Dobricic, V; Fogel, BL; Garcia-Estevez, D; Goldman, J; Goudreau, JL; Hopfer, S; Jankovic, M; Jauma, S; Jen, JC; Kirdlarp, S; Klepper, J; Kostic, V; Lang, AE; Linglart, A; Maisenbacher, MK; Manyam, BV; Mazzoni, P; Miedzybrodzka, Z; Mitarnun, W; Mitchell, PB; Mueller, J; Novakovic, I; Paucar, M; Paulson, H; Simpson, SA; Svenningsson, P; Tuite, P; Vitek, J; Wetchaphanphesat, S; Williams, C; Yang, M; Schofield, PR; de Oliveira, JRM; Sobrido, MJ; Geschwind, DH; Coppola, G
Source
Neurogenetics. 14(1):11-22
Subject
Language
English
English
English
ISSN
1364-6753