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