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]
- Brain : a journal of neurology Sep 2004
- 1979-92 p. digital
Publication Type: Journal Article
1460-2156
10.1093/brain/awh216 doi
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