Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds-Reference-Cited by-同舟云学术

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Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds

Published:2010-07-28 Issue:11 Volume:81 Page:1229-1232
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:Journal of Neurology, Neurosurgery & Psychiatry

Author:

Bauer P.,Stevanin G.,Beetz C.,Synofzik M.,Schmitz-Hubsch T.,Wullner U.,Berthier E.,Ollagnon-Roman E.,Riess O.,Forlani S.,Mundwiller E.,Durr A.,Schols L.,Brice A.

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Cited by 46 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Spinocerebellar ataxia type 11 (SCA11): An update;European Journal of Neuroscience;2023-06-16

2. Spinocerebellar ataxia type 11 (SCA11): TTBK2 variants, functions and associated disease mechanisms;The Cerebellum;2023-03-09

3. TTBK2mutations associated with spinocerebellar ataxia type 11 disrupt peroxisome dynamics and ciliary localization of SHH signaling proteins;2023-02-01

4. Autosomal Dominant Spinocerebellar Ataxias and Episodic Ataxias;Handbook of the Cerebellum and Cerebellar Disorders;2021-12-05

5. Spinocerebellar ataxias (SCAs) caused by common mutations;neurogenetics;2021-08-16

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