Chromosome 16q22.1-linked autosomal dominant cerebellar ataxia: An autopsy case report with some new observations on cerebellar pathology
Author:
Publisher
Wiley
Subject
Clinical Neurology,General Medicine,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-1789.2008.00947.x/fullpdf
Reference16 articles.
1. A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III;Owada;Neurology,2005
2. On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCA;Ishikawa;Neuropathology,2006
3. A modified impregnation method for staining apical dendrite and spine (Golgi modification method);Kelemen;Brain Nerve,1977
4. Spinocerebellar ataxia type 6. Gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset;Gomez;Ann Neurol,1997
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