This disease has been recently renamed as, “spinocerebellar ataxia type 31 (SCA31)”.
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
The 50th Anniversary of Japanese Society of Neuropathology
Version of Record online: 27 JUL 2010
© 2010 Japanese Society of Neuropathology
Volume 30, Issue 5, pages 490–494, October 2010
How to Cite
Ishikawa, K. and Mizusawa, H. (2010), 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. Neuropathology, 30: 490–494. doi: 10.1111/j.1440-1789.2010.01142.x
- Issue online: 27 JUL 2010
- Version of Record online: 27 JUL 2010
- Received 7 March 2010; revised 13 May 2010 and accepted 14 May 2010; published online 27 July 2010.
- 7Autosomal dominant cerebellar ataxia linked to chromosome 16q22.1with deafness is associated with a single nucleotide substitution in the 5′-untranslated region of the gene encoding a novel protein with spectrin repeat and Rho guanine-nucleotide exchange factor domains. Am J Hum Genet 2005; 77: 377–387., , et al.
- 8A comparative immunocytochemical study of human cerebellar cortex in X-chromosome-linked copper malabsorption (Menkes' kinky hair disease) and granule cell type cerebellar degeneration. Neuropathol Appl Neurobiol 1989; 15: 419–431., , .
- 10GrahamDI, LantosPL, eds. Greenfield's Neuropathology, 7th edn. 2. London: Arnold, 2002.