Spinocerebellar ataxia type 7: A distinctive form of autosomal dominant cerebellar ataxia with retinopathy and marked genetic anticipation

2001 ◽  
Vol 37 (1) ◽  
pp. 81-84 ◽  
Author(s):  
PJ Grattan-Smith ◽  
S Healey ◽  
JR Grigg ◽  
J Christodoulou
2008 ◽  
Vol 7 (2) ◽  
pp. 184-188 ◽  
Author(s):  
Caterina Mariotti ◽  
Alfredo Brusco ◽  
Daniela Di Bella ◽  
Claudia Cagnoli ◽  
Marco Seri ◽  
...  

2008 ◽  
Vol 66 (3b) ◽  
pp. 691-694 ◽  
Author(s):  
Hélio A.G. Teive ◽  
Renato Puppi Munhoz ◽  
Salmo Raskin ◽  
Lineu César Werneck

Spinocerebellar ataxia type 6 (SCA 6) is an autosomal dominant cerebellar ataxia caused by CAG repeat expansion in the SCA6 gene, a alpha 1A voltage-dependent calcium channel subunit gene on chromosome 19p13. SCA-6 is characterized predominantly by slowly progressive pure cerebellar ataxia with late onset. We report three index patients, with pure, late onset, cerebellar ataxia, belonging to three different Brazilian families, all of them with Japanese ancestry, from Hokkaido island of Japan.


2000 ◽  
Vol 67 (1) ◽  
pp. 229-235 ◽  
Author(s):  
Alexandra Herman-Bert ◽  
Giovanni Stevanin ◽  
Jean-Claude Netter ◽  
Olivier Rascol ◽  
David Brassat ◽  
...  

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