Cloning of the DMD Gene*
- 1 February 2005
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 76 (2) , 205-214
- https://doi.org/10.1086/428143
Abstract
No abstract availableThis publication has 55 references indexed in Scilit:
- Systemic delivery of human microdystrophin to regenerating mouse dystrophic muscle by muscle progenitor cellsProceedings of the National Academy of Sciences, 2004
- Functional improvement of dystrophic muscle by myostatin blockadeNature, 2002
- Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx miceJournal of Clinical Investigation, 1999
- β–sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complexNature Genetics, 1995
- Detection of 98% of DMD/BMD gene deletions by polymerase chain reactionHuman Genetics, 1990
- Duchenne muscular dystrophy: Deficiency of dystrophin at the muscle cell surfaceCell, 1988
- Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptideNature, 1988
- A cDNA clone from the Duchenne/Becker muscular dystrophy geneNature, 1987
- Long-range restriction map around the Duchenne muscular dystrophy geneNature, 1986
- PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPsThe Lancet, 1985