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Article

Association between a novel mutation in SLC20A2 and familial idiopathic basal ganglia calcification.

PloS one - 1 Jan 2013

Zhang Yang, Guo Xianan, Wu Anhua

Abstract excerpt

Familial idiopathic basal ganglia calcification (FIBGC) is a rare, autosomal dominant disorder involving bilateral calcification of the basal ganglia. To identify gene mutations related to a Chinese FIBGC lineage, we evaluated available individuals in the family using CT scans. DNA was extracted from the peripheral blood of available family members, and both exonic and flanking intronic sequences of the SLC20A2...

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Identifiers

PMID: 23437308
DOI: 10.1371/journal.pone.0057060
PMCID: PMC3577762

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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