A novel splice site mutation (3157+1G>T) in the dystrophin gene causing total exon skipping and DMD phenotype.

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)239
Number of pages1
JournalHuman Mutation
Volume17
Issue number3
Publication statusPublished - Mar 2001

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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