The chromosome 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA*): A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell-Reference-Cited by-同舟云学术

The chromosome 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA*): A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell

Published:2010-07-27 Issue: Volume: Page:no-no
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:

Author:

Ishikawa Kinya,Mizusawa Hidehiro

Publisher

Wiley

Subject

Clinical Neurology,General Medicine,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-1789.2010.01142.x/fullpdf

Reference14 articles.

1. The hereditary spinocerebellar ataxias in Japan;Sasaki;Cytogenet Genome Res,2003

2. A gene on SCA4 locus causes dominantly-inherited pure cerebellar ataxia;Nagaoka;Neurology,2000

3. Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1;Flanigan;Am J Hum Genet,1996

4. A clinical, genetic and neuropathologic study in a family with 16q-linked ADCA type III;Owada;Neurology,2005

5. On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q2.1-linked ADCA;Ishikawa;Neuropathology,2006

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