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Article

3' Acceptor splice site mutation in intron 50 leads to mild Duchenne muscular dystrophy phenotype.

Human mutation - 1 Jan 1998

Kekou K, Florentin L, Metaxotou C

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Identifiers

PMID: 9452089
DOI: 10.1002/humu.1380110168

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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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