A symptomatic female patient with Duchenne muscular dystrophy diagnosed by dystrophin-staining: A case report
- 1 January 1992
- journal article
- case report
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 151 (1), 66-68
- https://doi.org/10.1007/bf02073897
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Negative dystrophin staining in muscles of patients with complex glycerol kinase deficiencyThe Journal of Pediatrics, 1990
- Dystrophin diagnosis: comparison of dystrophin abnormalities by immunofluorescence and immunoblot analyses.Proceedings of the National Academy of Sciences, 1989
- Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locusHuman Genetics, 1989
- Duchenne Muscular Dystrophy Manifesting CarriersArchives of Neurology, 1989
- ABSENCE OF DYSTROPHIN IN BECKER MUSCULAR DYSTROPHYThe Lancet, 1989
- MYOPATHY IN COMPLEX GLYCEROL KINASE-DEFICIENCY PATIENTS IS DUE TO 3' DELETIONS OF THE DYSTROPHIN GENE1988
- Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptideNature, 1988
- CLINICAL CONCEPTS OF DUCHENNE MUSCULAR DYSTROPHYBrain, 1988
- Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individualsCell, 1987
- [Cardiomyopathy in female carriers of the Duchenne gene].1984