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Article

SQSTM1 mutations in Han Chinese populations with sporadic amyotrophic lateral sclerosis.

Neurobiology of aging - 1 Mar 2014

Chen Yongping, Zheng Zhen-Zhen, Chen Xueping, Huang Rui, Yang Yuan, Yuan Lixing, Pan Lei, Hadano Shinji, Shang Hui-Fang

Abstract excerpt

Mutations in the sequestosome 1 gene (SQSTM1) have recently been identified in patients with amyotrophic lateral sclerosis, accounting for 1.11%-4.92% of familial ALS and 2.42%-4.37% of sporadic amyotrophic lateral sclerosis (SALS). The mutation spectrum of SQSTM1 in Chinese patients with SALS remains unknown. Three hundred and six patients with SALS from the Department of Neurology, West China Hospital of...

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Identifiers

PMID: 24138988
DOI: 10.1016/j.neurobiolaging.2013.09.008

Genes

SQSTM1

Variants

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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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