Fingerprint
Dive into the research topics of 'Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
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 Goldman
*Corresponding author for this work
- Childrens Hosp Westmead, Children's Medical Research Institute - Australia, Inst Neurosci & Muscle Res
- University of California at Los Angeles
- Fdn Publ Galega Med Xenom
- University of Santiago de Compostela
- Universidade Federal de Pernambuco
- Inst Hlth Carlos III, Ctr Biomed Res Rare Dis CIBERER
- Universidade de São Paulo
- University of New South Wales
- University of New Mexico
- Woodinville Psychiat Assoc
- University of Minnesota Twin Cities
- Hosp Figueres, Dept Neurol
- University Clinical Center, Belgrade
- Monforte de Lemos Hosp SERGAS, Dept Neurol
- Columbia University
- Michigan State University
- University of Barcelona
- Buriram Hosp, Div Med
- Klinikum Aschaffenburg
- University of Toronto
- Institut national de la santé et de la recherche médicale
- Florida State University
- Pennsylvania State University
- Black Dog Inst
- Karolinska Institutet
- University of Michigan, Ann Arbor
- Semel Institute for Neuroscience and Human Behavior
Research output: Contribution to journal › Article › peer-review
124
Citations
(Scopus)