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
*Corresponding author for this work
- David Geffen School of Medicine at UCLA
- Clinical University Hospital
- Federal University of Pernambuco
- Centro de Investigación Biomédica en Red (CIBER) de Enfermedades Raras, CIBERER
- Cedars-Sinai Medical Center
- Johns Hopkins University
- University of Sao Paulo
- Neuroscience Research Australia
- School of Medical Sciences
- University of New Mexico
- Woodinville Psychiatric Association
- Macquarie University, Australian School of Advanced Medicine
- Monforte de Lemos Hospital-SERGAS
- Columbia University Medical Center
- Michigan State University
- Hospital Universitari de Bellvitge
- Buriram Hospital
- Children's Hospital Aschaffenburg
- University Health Network
- AP-HP Assistance Publique - Hopitaux de Paris
- University of Florida
- Pennsylvania State University
- University of Aberdeen
- Karolinska Institutet
- University of Michigan
- University of Minnesota Medical School
- California State University Los Angeles
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