Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Association between rare UBQLN2 variants and amyotrophic lateral sclerosis in Chinese population].

Zhonghua yi xue za zhi - 30 Mar 2021

Chen J Y, Liu X Y, Xu Y S, Fan D S

Abstract excerpt

Objective: To explore the association between rare UBQLN2 variants and amyotrophic lateral sclerosis (ALS) in Chinese population, and the characteristic of phenotypes of their carriers. Methods: A total of 166 ALS patients who visited Department of Neurology of Peking University Third Hospital between January 2018 and July 2020 were recruited. The next-generation sequencing was performed to screen possible...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adaptor Proteins, Signal Transducing
Share to Amyotrophic Lateral Sclerosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Autophagy-Related Proteins

Share to Cell Cycle Proteins

Share to Mutation

Share to Ubiquitins

Source

Identifiers

PMID: 33789365
DOI: 10.3760/cma.j.cn112137-20201015-02835

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Association between rare UBQLN2 variants and amyotrophic lateral sclerosis in Chinese population].PMID 33789365Read ↗

[Rare variants of HSPB1 are probably associated with amyotrophic lateral sclerosis].Semantic proximity Read ↗

Role of genetics in amyotrophic lateral sclerosis: a large cohort study in Chinese mainland population.Semantic proximity Read ↗

Clinical and genetic characteristics of 1672 cases of amyotrophic lateral sclerosis in China: a single-center retrospective study.Semantic proximity Read ↗

Incidence of amyotrophic lateral sclerosis-associated genetic variants: a clinic-based study.Semantic proximity Read ↗

Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral SclerosisSemantic proximity Read ↗

A case study of comprehensive association analysis and risk prediction of amyotrophic lateral sclerosis in a Chinese population.Semantic proximity Read ↗

Characterising the Genetic Landscape of Amyotrophic Lateral Sclerosis: A Catalogue and Assessment of Over 1,000 Published Genetic VariantsSemantic proximity Read ↗

Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese.Semantic proximity Read ↗

A genome-wide association study on amyotrophic lateral sclerosis in the Taiwanese Han population.Semantic proximity Read ↗

Clinical and genetic features of patients with amyotrophic lateral sclerosis in southern China.Semantic proximity Read ↗

Rare neurological and neurodevelopmental variants in ALS link to onset, survival and family historySemantic proximity Read ↗

Two new cases with the UBQLN2 gene mutation in Han Chinese.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.