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Article

Preliminary Results of a Genetic Study of Children with Duchenne Myodystrophy in Aktobe, Kazakhstan.

Archives of Razi Institute - 1 Jun 2023

Umurzakova A, Ayaganov D, Mannapova A, Dzhumasheva B, Dzhaksybayeva A

Abstract excerpt

Duchenne muscular dystrophy (DMD) is an X-linked recessive neuromuscular illness with a progressive course caused by mutations in the gene encoding the protein dystrophin (DMD; locus Xp21. 2). This study aimed to investigate the clinical aspects of DMD progression according to the mutation type. Included in the study were 38 boys aged 3 to 11 years. Laboratory (biochemical evaluation of the level of creatinine...

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Identifiers

PMID: 38028863
DOI: 10.22092/ARI.2022.360050.2534
PMCID: PMC10657926

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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.

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