Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31 - Nygaard, Torbjoern G.; Raymond, Deborah; Chen, Caiping; Nishino, Ichizo; Greene, Paul E.; Jennings, Danna; Heiman, Gary A.; Klein, Christine; Saunders-Pullman, Rachel J.; Kramer, Patricia; Ozelius, Laurie J.; Bressman, Susan B. (Annals of neurology, 1999)
Keywords: Adolescent; Adult; Age of Onset; Aged; Biological and medical sciences; Cell Line; Chromosome Mapping; Chromosomes, Human, Pair 11; Chromosomes, Human, Pair 17; DNA - blood; Dystonia - genetics; Female; Genetic Linkage; Genetic Markers; Genotype; Humans; Male; Medical sciences; Middle Aged; Myoclonus - genetics; Nervous system (semeiology, syndromes); Nervous system as a whole; Neurology; Pedigree; Human; Nervous system diseases; Linkage; Myoclonus; Family study; Exploration; Chromosome C7; Involuntary movement; Genetic disease; Striated muscle disease; Genetics; Dystonia; Neurological disorder; Extrapyramidal syndrome