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Article

Gigaxonin mutation analysis in patients with NIFID.

Neurobiology of aging - 1 Aug 2011

Dequen Florence, Cairns Nigel J, Bigio Eileen H, Julien Jean-Pierre

Abstract excerpt

Neuronal intermediate filament inclusion disease (NIFID) is a frontotemporal lobar degeneration (FTLD) characterized by frontotemporal dementia (FTD), pyramidal and extrapyramidal signs. The disease is histologically characterized by the presence of abnormal neuronal cytoplasmic inclusions (NCIs)...

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Source

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Identifiers

PMID: 19782434
DOI: 10.1016/j.neurobiolaging.2009.08.018
PMCID: PMC2987523

Genes

GAN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19782434-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Gigaxonin mutation analysis in patients with NIFID.PMID 19782434Read ↗

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