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Article

Novel 3678delA mutation in exon 26 of the dystrophin gene causing Duchenne muscular dystrophy.

Human mutation - 1 Jan 1998

Agarwal-Mawal A, Vanasse M, Simard L R

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Source

Identifiers

PMID: 9452029
DOI: 10.1002/humu.1380110108

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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Novel 3678delA mutation in exon 26 of the dystrophin gene causing Duchenne muscular dystrophy.PMID 9452029Read ↗

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Recurrent nonsense p.Trp3416* variant in the DMD gene identified in healthy Lebanese individuals: Implications for variant classification and genotype-phenotype correlations.Semantic proximity Read ↗

Novel mutations and polymorphisms in the human dystrophin gene detected by double-strand conformation analysis.Semantic proximity Read ↗

Commentary on 'Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center'.Semantic proximity Read ↗

A Deletion in Duchenne Muscular Dystrophy Gene Found Through Whole Exome Sequencing in Iran.Semantic proximity Read ↗

Splicing mutation of a gene within the Duchenne muscular dystrophy family.Semantic proximity Read ↗

A dynamic trinucleotide repeat (TNR) expansion in the DMD geneSemantic proximity Read ↗

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