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Article

2q37 as a susceptibility locus for idiopathic basal ganglia calcification (IBGC) in a large South Tyrolean family.

Journal of molecular neuroscience : MN - 1 Nov 2009

Volpato Claudia Béu, De Grandi Alessandro, Buffone Ebba, Facheris Maurizio, Gebert Uwe, Schifferle Günther, Schönhuber Rudolf, Hicks Andrew, Pramstaller Peter P

Abstract excerpt

Familial idiopathic basal ganglia calcification (FIBGC) is an inherited neurodegenerative disorder characterized by the accumulation of calcium deposits in different brain regions, particularly in the basal ganglia. FIBGC usually follows an autosomal dominant pattern of inheritance. Despite the mapping to chromosome 14q of a susceptibility locus for IBGC (IBCG1) in one family, this locus has been excluded in...

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Identifiers

PMID: 19757205
DOI: 10.1007/s12031-009-9287-3

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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2q37 as a susceptibility locus for idiopathic basal ganglia calcification (IBGC) in a large South Tyrolean family.PMID 19757205Read ↗

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Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification.Semantic proximity Read ↗

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