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1999 | 1 |
2013 | 1 |
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Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.
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.
Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease).
Geschwind DH, Loginov M, Stern JM.
Geschwind DH, et al.
Am J Hum Genet. 1999 Sep;65(3):764-72. doi: 10.1086/302558.
Am J Hum Genet. 1999.
PMID: 10441584
Free PMC article.
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