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

Genotype and age at diagnosis in Thai boys with Duchenne muscular dystrophy (DMD).

Neuromuscular disorders : NMD - 1 Oct 2020

Yamputchong Pattareeya, Pho-Iam Theeraphong, Limwongse Chanin, Wattanasirichaigoon Duangrurdee, Sanmaneechai Oranee

Abstract excerpt

Gene-based therapy is a treatment for Duchenne muscular dystrophy (DMD) has become lately available; limited use for specific of mutation and percentages of the patients. Diagnosis in Thailand is made by muscle biopsy or multiplex ligation-dependent probe amplification (MLPA). Appropriate treatment in developing countries is difficult because gene sequencing is expensive and has limited availability. We aimed to...

Read the complete abstract on PubMed

Topics

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

Share to Age Factors
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Association Studies

Share to Genetic Testing

Share to Infant

Share to Multiplex Polymerase Chain Reaction

Share to Muscular Dystrophy, Duchenne

Share to Thailand

Source

Identifiers

PMID: 32962870
DOI: 10.1016/j.nmd.2020.09.003

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genotype and age at diagnosis in Thai boys with Duchenne muscular dystrophy (DMD).PMID 32962870Read ↗

Characteristics of Disease Progression and Genetic Correlation in Ambulatory Iranian Boys With Duchenne Muscular DystrophySemantic proximity Read ↗

Utilisation of exome sequencing for muscular disorders in Thai paediatric patients: diagnostic yield and mutational spectrum.Semantic proximity Read ↗

Utilisation of Exome Sequencing for Muscular Disorders in Thai Paediatric Patients: Diagnostic Yield and Mutational SpectrumSemantic proximity Read ↗

[Clinical practice guidelines for Duchenne muscular dystrophy].Semantic proximity Read ↗

Sensitivity and frequencies of dystrophin gene mutations in Thai DMD/BMD patients as detected by multiplex PCR.Semantic proximity Read ↗

Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patientsSemantic proximity Read ↗

Genetic Identification of DMD Gene Pathogenic Mutations: Retrospective Genetic Analysis of 507 Patients Based on Next-Generation SequencingSemantic proximity Read ↗

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

The importance of genetic diagnosis for Duchenne muscular dystrophySemantic proximity Read ↗

Targeted sequencing of the DMD locus: A comprehensive diagnostic tool for all mutations.Semantic proximity Read ↗

Mutation spectrum analysis of Duchenne/Becker muscular dystrophy in 68 families in Kuwait: The era of personalized medicineSemantic proximity Read ↗

Genetic Variation Analysis and Treatment Strategy of 20 Patients with Dystrophin Gene MutationsSemantic proximity Read ↗

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