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

SCA38 is rare in Mainland China.

Journal of the neurological sciences - 15 Nov 2015

Liu Zhen, Zeng Sheng, Zeng Junsheng, Zhou Yao, Zeng Xianfeng, Jiang Hong, Shen Lu, Tang Beisha, Wang Junling

Abstract excerpt

Spinocerebellar ataxias (SCAs) are a group of dominantly inherited neurodegenerative disorders distributed worldwide. Nearly 35 SCAs have been localized and 28 genes have been identified. Recently, mutations in the elongation of a very long chain fatty acids-5 gene (ELOVL5) were reported to cause a SCA38 subtype. To describe the epidemiology of SCA38 in Mainland China, we analyzed the coding sequence of ELOVL5 in...

Read the complete abstract on PubMed

Topics

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

Share to Acetyltransferases
Share to China
Share to Fatty Acid Elongases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Sequence Analysis, DNA

Share to Spinocerebellar Ataxias

Source

Identifiers

PMID: 26433464
DOI: 10.1016/j.jns.2015.09.350

Genes

ELOVL5

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

SCA38 is rare in Mainland China.PMID 26433464Read ↗

ELOVL5 mutations cause spinocerebellar ataxia 38.Semantic proximity Read ↗

Spinocerebellar ataxia type 28 (SCA28) is an uncommon cause of dominant ataxia among Chinese kindreds.Semantic proximity Read ↗

Spinocerebellar ataxias in mainland China: an updated genetic analysis among a large cohort of familial and sporadic cases.Semantic proximity Read ↗

Spinocerebellar ataxias in Asia: Prevalence, phenotypes and management.Semantic proximity Read ↗

Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China.Semantic proximity Read ↗

Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four families.Semantic proximity Read ↗

Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern SpainSemantic proximity Read ↗

Docosahexaenoic acid is a beneficial replacement treatment for spinocerebellar ataxia 38.Semantic proximity Read ↗

Spinocerebellar ataxia type 36 in the Han ChineseSemantic proximity Read ↗

Genetic and clinical profiles in a large cohort of Chinese individuals with spinocerebellar ataxia type 1Semantic proximity Read ↗

A Novel Mutation in ELOVL4 Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia: A Broadened Spectrum of SCA34.Semantic proximity Read ↗

A family study and literature review of ELOVL4-associated spinocerebellar ataxia type 34Semantic proximity Read ↗

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