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Article

Carrier detection in Duchenne muscular dystrophy using molecular methods.

The Indian journal of medical research - 1 Jun 2013

Sakthivel Murugan S M, Arthi C, Thilothammal N, Lakshmi B R

Abstract excerpt

BACKGROUND & OBJECTIVES: Duchenne and Becker muscular dystrophies are X-linked allelic disorders which are caused by mutations in the DMD gene. Carrier analysis in DMD is complicated due to the heterozygous nature of the X chromosome. Several techniques have been tried for carrier analysis in families where the mutation is identified including quantitative multiplex PCR (qmPCR), Southern blot, and now multiplex...

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Share to Chromosomes, Human, X
Share to Dystrophin

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Gene Deletion

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Share to Muscular Dystrophy, Duchenne

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Source

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Identifiers

PMID: 23852291
PMCID: PMC3734715

Genes

DMD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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