Duchenne-Becker Muscular Dystrophy and the Nondystrophic Myotonias
- 1 November 1993
- journal article
- review article
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 50 (11) , 1227-1237
- https://doi.org/10.1001/archneur.1993.00540110101010
Abstract
From JAMA Neurology — Duchenne-Becker Muscular Dystrophy and the Nondystrophic Myotonias — Paradigms for Loss of Function and Change of Function of Gene ProductsKeywords
This publication has 52 references indexed in Scilit:
- 243 Genotype/phenotype correlations in Duchenne/Becker muscular dystrophyEuropean Journal of Paediatric Neurology, 1999
- Localization of dystrophin gene transcripts during mouse embryogenesis.The Journal of cell biology, 1992
- Point mutations and polymorphisms in the human dystrophin gene identified in genomic DNA sequences amplified by multiplex PCRHuman Genetics, 1992
- Point mutations in the dystrophin gene.Proceedings of the National Academy of Sciences, 1992
- Cell and fiber type distribution of dystrophinNeuron, 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
- Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy geneNature, 1986
- Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.Proceedings of the National Academy of Sciences, 1985