Machado-Joseph Disease
Abstract
The frequency, and clinical, molecular, and neuropathological features of spinocerebellar ataxia 3 (SCA3) and Machado-Joseph disease (MJD) in 125 autosomal dominant cerebellar ataxia (ADCA) families were analyzed at the Service de Neuropathologie, Hopital de la Salpetriere, Paris, and Service de Neurologie, Hopital de Haut Leveque, Pessac, France; and Service de Neurologie, Hopital des Specialites, Rabat, Morocco.
DOI: https://doi.org/10.15844/pedneurbriefs-10-6-11 | Journal eISSN: 2166-6482
Language: English
Page range: 48 - 48
Published on: Jun 1, 1996
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 1996 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.