Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.
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Hsu SC, et al. Among authors: lemos rr.
Neurogenetics. 2013 Feb;14(1):11-22. doi: 10.1007/s10048-012-0349-2. Epub 2013 Jan 20.
Neurogenetics. 2013.
PMID: 23334463
Free PMC article.