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Article

Carrier detection by microsatellite analysis of Duchenne/Becker muscular dystrophy in Hungarian families.

Annals of human genetics - 1 Nov 1998

Bachrati C Z, Somodi Z, Endreffy E, Kalmár T, Raskó I

Abstract excerpt

Duchenne and Becker muscular dystrophies are among the most severe and frequent inherited disorders. Being still incurable, medical treatment is concentrated on the carrier diagnosis of the members of the affected families. Here we report the results of the studies of 151 members of 41 Hungarian families, obtained with multiplex PCR amplification of 18 exons as well as the muscle specific promoter region, and...

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Identifiers

PMID: 10363129
DOI: 10.1046/j.1469-1809.1998.6260511.x

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

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