The muscular dystrophies
- 31 December 1997
- journal article
- Published by Elsevier in European Journal of Paediatric Neurology
- Vol. 1 (1) , 53-54
- https://doi.org/10.1016/s1090-3798(97)80013-x
Abstract
No abstract availableThis publication has 32 references indexed in Scilit:
- SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin functionHuman Molecular Genetics, 1995
- Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophyNature Genetics, 1994
- Location of facioscapulohumeral muscular dystrophy gene on chromosome 4The Lancet, 1990
- Mapping of the Emery-Dreifuss gene through reconstruction of crossover points in two Italian pedigreesHuman Genetics, 1988
- Characterization of Dystrophin in Muscle-Biopsy Specimens from Patients with Duchenne's or Becker's Muscular DystrophyNew England Journal of Medicine, 1988
- The complete sequence of dystrophin predicts a rod-shaped cytoskeletal proteinCell, 1988
- Dystrophin: The protein product of the duchenne muscular dystrophy locusCell, 1987
- Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individualsCell, 1987
- A cDNA clone from the Duchenne/Becker muscular dystrophy geneNature, 1987
- Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy geneNature, 1986