Genetics of movement disorders
- 1 August 1996
- journal article
- review article
- Published by Wolters Kluwer Health in Current Opinion in Neurology
- Vol. 9 (4) , 290-297
- https://doi.org/10.1097/00019052-199608000-00009
Abstract
Trinucleotide repeat expansions or unstable mutations are the cause of a growing number of hereditary movement disorders, especially inherited ataxias. Diagnostic practice as well as disease classifications have altered accordingly. Genes responsible for 'Parkinsonian plus' syndromes and episodic movement disorders have also been recently mapped.Keywords
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