A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24. [electronic resource]
Producer: 20041015Description: 1979-92 p. digitalISSN:- 1460-2156
- Adult
- Age of Onset
- Aged
- Chromosome Mapping -- methods
- Chromosomes, Human, Pair 15 -- genetics
- Dementia -- complications
- Female
- Genetic Linkage -- genetics
- Humans
- Magnetic Resonance Imaging
- Male
- Middle Aged
- Muscle Weakness -- etiology
- Muscle, Skeletal -- pathology
- Myosin Heavy Chains -- analysis
- Myotonic Disorders -- complications
- Pedigree
- Phenotype
- RNA-Binding Proteins -- genetics
- Sex Ratio
- tau Proteins -- analysis
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Publication Type: Journal Article
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