Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

Sandy Chan Hsu, Renee L. Sears, Roberta R. Lemos, Beatriz Quintans, 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 Dobricic, Brent L. Fogel, Daniel Garcia-Estevez, Jill GoldmanJohn L. Goudreau, Suellen Hopfer, Milena Jankovic, Serge Jauma, Joanna C. Jen, Suppachok Kirdlarp, Joerg Klepper, Vladimir Kostic, Anthony E. Lang, Agnes Linglart, Melissa K. Maisenbacher, Bala V. Manyam, Pietro Mazzoni, Zofia Miedzybrodzka, Witoon Mitarnun, Philip B. Mitchell, Jennifer Mueller, Ivana Novakovic, Martin Paucar, Henry Paulson, Sheila A. Simpson, Per Svenningsson, Paul Tuite, Jerrold Vitek, Suppachok Wetchaphanphesat, Charles Williams, Michele Yang, Peter R. Schofield, Joao R. M. de Oliveira, Maria-Jesus Sobrido, Daniel H. Geschwind, Giovanni Coppola*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

122 Citations (Scopus)

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