The genetic basis of neuromuscular disorders
- 31 August 1996
- journal article
- review article
- Published by Elsevier in Trends in Genetics
- Vol. 12 (8) , 294-298
- https://doi.org/10.1016/0168-9525(96)10033-0
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- Genetic, allelic and phenotypic heterogeneity of muscular dystrophies with primary and secondary involvement of adhalin (alpha-sarcoglycan)Neuromuscular Disorders, 1996
- A Cluster of Transposon-like Repetitive Sequences in Intron 7 of the Human Dystrophin GeneJournal of Molecular Biology, 1993
- The structural and functional diversity of dystrophinNature Genetics, 1993
- Two hot spots of recombination in the DMD gene correlate with the deletion prone regionsHuman Molecular Genetics, 1992
- A transposon-like element in the deletion-prone region of the dystrophin geneGenomics, 1992
- Partial gene duplication as a cause of human diseaseHuman Mutation, 1992
- Sequences of junction fragments in the deletion-prone region of the dystrophin geneGenomics, 1991
- High resoluation deletion breakpoint mapping in the DMD gene by whole cosmid hybridizationNucleic Acids Research, 1989
- An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locusGenomics, 1988
- Mutation rate in Duchenne type of muscular dystrophy.Journal of Medical Genetics, 1970