Response to: “The Pathophysiology and Clinical Manifestations of Spinocerebellar Ataxia Type 6” Commentary by Rowland et al.

2021 ◽  
Author(s):  
Zubir Rentiya ◽  
Robert Hutnik ◽  
Junun Bae
2020 ◽  
Vol 19 (3) ◽  
pp. 459-464 ◽  
Author(s):  
Zubir Rentiya ◽  
Robert Hutnik ◽  
Yolunna Q Mekkam ◽  
Junun Bae

Gene ◽  
2006 ◽  
Vol 380 (1) ◽  
pp. 54-61 ◽  
Author(s):  
Eva Andrés-Mateos ◽  
Jesús Cruces ◽  
Jaime Renart ◽  
Luisa M. Solís-Garrido ◽  
Rocío Serantes ◽  
...  

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.


2001 ◽  
Vol 185 (1) ◽  
pp. 43-47 ◽  
Author(s):  
Masatada Mori ◽  
Yoshiki Adachi ◽  
Masayoshi Kusumi ◽  
Kenji Nakashima

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