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Article

p62/SQSTM1 analysis in frontotemporal lobar degeneration.

Neurobiology of aging - 1 Mar 2015

Miller Louise, Rollinson Sara, Callister Janis Bennion, Young Kate, Harris Jenny, Gerhard Alex, Neary David, Richardson Anna, Snowden Julie, Mann David M A, Pickering-Brown Stuart M

Abstract excerpt

Mutations in the gene p62/SQSTM1 have been reported as a relatively rare cause of frontotemporal lobar degeneration (FTLD). To establish whether this was the case for cases of FTLD from the United Kingdom, we sequenced the sequenced the entire open reading frame of this gene in a large cohort of...

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Source

Identifiers

PMID: 25433461
DOI: 10.1016/j.neurobiolaging.2014.08.035

Genes

SQSTM1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25433461-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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