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Article

Serum Levels of MicroRNA-206 and Novel Mini-STR Assays for Carrier Detection in Duchenne Muscular Dystrophy.

International journal of molecular sciences - 13 Aug 2016

Anaya-Segura Mónica Alejandra, Rangel-Villalobos Héctor, Martínez-Cortés Gabriela, Gómez-Díaz Benjamín, Coral-Vázquez Ramón Mauricio, Zamora-González Edgar Oswaldo, García Silvia, López-Hernández Luz Berenice

Abstract excerpt

Duchenne Muscular Dystrophy (DMD) is an X-linked neuromuscular disorder in which the detection of female carriers is of the utmost importance for genetic counseling. Haplotyping with polymorphic markers and quantitation of creatine kinase levels (CK) allow tracking of the at-risk haplotype and evidence muscle damage, respectively. Such approaches are useful for carrier detection in cases of unknown mutations. The...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 27529242
DOI: 10.3390/ijms17081334
PMCID: PMC5000731

Genes

DMD

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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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