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Article

[Microsatellite analysis of Duchenne muscular dystrophy].

Nihon rinsho. Japanese journal of clinical medicine - 1 Dec 1997

Fujishita S, Shibuya N

Abstract excerpt

Duchenne muscular dystrophy is X-linked recessive neuromuscular disorders caused by mutations in the dystrophin gene. Prenatal diagnosis and carrier detection are usually performed using diallelic RFLP-markers which are not always informative. Now 30 of microsatellite marker have reported, these microsatellite polymorphism can easily be amplified using PCR technique. If mutations are known to localize in this...

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Source

Identifiers

PMID: 9436423

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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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[Microsatellite analysis of Duchenne muscular dystrophy].PMID 9436423Read ↗

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