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

Duchenne or Becker muscular dystrophy: a clinical, genetic and immunohistochemical study in China.

Neurology India - 1 Jan 2000

Wang Qian, Yang Xiaofeng, Yan Yang, Song Nan, Lin Changkun, Jin Chunlian

Abstract excerpt

BACKGROUND AND OBJECTIVE: Duchenne and Becker muscular dystrophies are X-linked diseases caused by mutations in the dystrophin gene, which affect approximately 1 in 3,500 and 1 in 18,000 boys, respectively. The aim of this work was to develop a method to assist the diagnosis and classification of the disease. MATERIALS AND METHODS: A large data set of dystrophin mutations was detected in 167 Chinese patients by...

Read the complete abstract on PubMed

Topics

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

Share to C-Reactive Protein
Share to China
Share to Dystrophin

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lymphoproliferative Disorders

Share to Microsatellite Repeats

Share to Muscle, Skeletal

Share to Muscular Dystrophy, Duchenne

Source

Identifiers

PMID: 22234188
DOI: 10.4103/0028-3886.91354

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

Duchenne or Becker muscular dystrophy: a clinical, genetic and immunohistochemical study in China.PMID 22234188Read ↗

Genetic analysis of 1051 Chinese families with Duchenne/Becker Muscular DystrophySemantic proximity Read ↗

Consecutive analysis of mutation spectrum in the dystrophin gene of 507 Korean boys with Duchenne/Becker muscular dystrophy in a single center.Semantic proximity Read ↗

Comprehensive genetic characteristics of dystrophinopathies in China.Semantic proximity Read ↗

Molecular Analysis-Based Genetic Characterization of a Cohort of Patients with Duchenne and Becker Muscular Dystrophy in Eastern China.Semantic proximity Read ↗

[Mutation analysis of 81 cases with Duchenne/Becker muscular dystrophy].Semantic proximity Read ↗

Mutational spectrum of Duchenne muscular dystrophy in Spain: Study of 284 cases.Semantic proximity Read ↗

Comprehensive analysis for genetic diagnosis of Dystrophinopathies in JapanSemantic proximity Read ↗

Molecular analysis of the dystrophin gene in 407 Chinese patients with Duchenne/Becker muscular dystrophy by the combination of multiplex ligation-dependent probe amplification and Sanger sequencing.Semantic proximity Read ↗

Genetic analysis of the dystrophin gene in children with Duchenne and Becker muscular dystrophies.Semantic proximity Read ↗

[Gene Mutation Spectrum Analysis of 170 Patients with Duchenne/Bayesian Muscular Dystrophy in Southwest of China].Semantic proximity Read ↗

Genomic insights into Duchene muscular dystrophy: Analysis of 1250 patients reveals 30% novel genetic patterns and 6 novel variantsSemantic proximity Read ↗

Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center.Semantic proximity Read ↗

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