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eNauka >  Results >  Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification
Title: Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification
Authors: Hsu, Sandy Chan; Sears, Renee L.; Lemos, Roberta R.; Quintáns, Beatriz; Huang, Alden; Spiteri, Elizabeth; Nevarez, Lisette; Mamah, Catherine; Zatz, Mayana; Pierce, Kerrie D.;
Issue Date: 2013
Publication: neurogenetics
ISSN: 1364-6745 Neurogenetics Search Idenfier
Type: Article
Collation: vol. 14 br. 1 str. 11-22
DOI: 10.1007/s10048-012-0349-2
WoS-ID: 000314762500002
Scopus-ID: 2-s2.0-84873738898
PMID: 23334463
PMCID: PMC4023541
URI: https://enauka.gov.rs/handle/123456789/545847
Metadata source: Migrirano iz RIS podataka
M-category: 
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