Publication
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification
Sandy Chan Hsu, Renee L. Sears, Roberta R. Lemos, Beatriz Quintáns, Alden Huang, Elizabeth Spiteri, Lisette Nevarez, Catherine Mamah, Mayana Zatz, Kerrie D. Pierce, Janice M. Fullerton, John C. Adair, Jon E. Berner, Matthew Bower, Henry Brodaty, Olga Carmona, Valerija Dobricić, Brent L. Fogel, Daniel García-Estevez, Jill Goldman, John L. Goudreau, Suellen Hopfer, Milena Janković, Serge Jaumà, Joanna C. Jen, Suppachok Kirdlarp, Joerg Klepper, Vladimir Kostić, Anthony E. Lang, Agnès Linglart, Melissa K. Maisenbacher, Bala V. Manyam, Pietro Mazzoni, Zofia Miedzybrodzka, Witoon Mitarnun, Philip B. Mitchell, Jennifer Mueller, Ivana Novaković, Martin Paucar, Henry Paulson, Sheila A. Simpson, Per Svenningsson, Paul Tuite, Jerrold Vitek, Suppachok Wetchaphanphesat, Charles Williams, Michele Yang, Peter R. Schofield, João R. M. de Oliveira, María-Jesús Sobrido, Daniel H. Geschwind, Giovanni Coppola
Neurogenetics, January 2013, Springer Science + Business Media
DOI: 10.1007/s10048-012-0349-2