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Updated: Oct 14, 2026

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Multi-exon Skipping Using Cocktail Antisense Oligonucleotides in the Canine X-linked Muscular Dystrophy
Published on: May 24, 2016
[Molecular biology in diagnosis and detection of deletion in Duchenne muscular dystrophy]
W Graninger1, W Wintersberger, G Meron
1II. Medizinische Universitätsklinik, Wien.
Wiener Klinische Wochenschrift
|January 1, 1991
Abstract:
For the purpose of carrier identification and genetic counselling we investigated deletions of the Duchenne muscular dystrophy (DMD) gene in three families of patients with Duchenne muscular dystrophy. Using a limited number of probes of the DMD cDNA in Southern blots, we detected a deletion in only one patient. Additional methodology is necessary to warrant reliable identification of carriers and exact prenatal diagnosis.

