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Article

Population and computational analysis of the MGEA6 P521A variation as a risk factor for familial idiopathic basal ganglia calcification (Fahr's disease).

Journal of molecular neuroscience : MN - 1 Mar 2011

Lemos Roberta R, Oliveira Danyllo F, Zatz Mayana, Oliveira João R M

Abstract excerpt

Familial idiopathic basal ganglia calcification, also known as "Fahr's disease" (FD), is a neuropsychiatric disorder with autosomal dominant pattern of inheritance and characterized by symmetric basal ganglia calcifications and, occasionally, other brain regions. Currently, there are three loci linked to this devastating disease. The first one (IBGC1) is located in 14q11.2-21.3 and the other two have been...

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Source

Identifiers

PMID: 20838928
DOI: 10.1007/s12031-010-9445-7

Genes

MAF
NRG1
SNTG1

Provenance

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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