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

[Analysis and application of SCA1 and SCA3/MJD gene CAG repeats in Han population in Northeastern China].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 1 Feb 2004

Jiang Miao, Jin Chun-lian, Lin Chang-kun, Qiu Guang-rong, Liu Zong-lan, Wang Chao-xiang, Sun Kai-lai

Abstract excerpt

OBJECTIVE: To investigate the normal range of (CAG)n in spinocerebellar ataxia type 1 (SCA1) gene and spinocerebellar ataxia type 3 (SCA3/MJD) gene in 110 normal subjects of Han population in Northeastern China, to assess the genotypes for clinically diagnosed spinocerebellar ataxia(SCA) individu...

Read the complete abstract on PubMed

Topics

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

Share to Ataxin-1
Share to Ataxin-3
Share to Ataxins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family Health

Share to Machado-Joseph Disease

Share to Spinocerebellar Ataxias

Share to Trinucleotide Repeat Expansion

Share to Trinucleotide Repeats

Source

Identifiers

PMID: 14767919

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-14767919-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Analysis and application of SCA1 and SCA3/MJD gene CAG repeats in Han population in Northeastern China].PMID 14767919Read ↗

[CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].Semantic proximity Read ↗

[Molecular and prenatal diagnosis of a pedigree with spinocerebellar ataxia].Semantic proximity Read ↗

[Gene diagnosis and CAG repeat analysis of spinocerebellar ataxia cases of Guangxi region].Semantic proximity Read ↗

[SCA1, SCA2, MJD/SCA3 (CAG)n mutation detection and analysis in patients with hereditary spinocerebellar ataxia from Chinese families].Semantic proximity Read ↗

[Polynucleotide repeat expansion of nine spinocerebellar ataxia subtypes and dentatorubral-pallidoluysian atrophy in healthy Chinese Han population].Semantic proximity Read ↗

[The study of clinical characteristics and molecular genetics in a large spinocerebellar ataxia3 pedigree].Semantic proximity Read ↗

Population genetics and new insight into range of CAG repeats of spinocerebellar ataxia type 3 in the Han Chinese population.Semantic proximity Read ↗

Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan.Semantic proximity Read ↗

[Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families].Semantic proximity Read ↗

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

[Analysis of SCA3/MJD3 gene mutation and genetic polymorphism in a guangxi family with spinocerebellar ataxia 3].Semantic proximity Read ↗

Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.Semantic proximity Read ↗

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