Mutations in the FGF14 gene are not a major cause of spinocerebellar ataxia in Caucasians-Reference-Cited by-同舟云学术

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Mutations in the FGF14 gene are not a major cause of spinocerebellar ataxia in Caucasians

Published:2004-09-13 Issue:5 Volume:63 Page:936-936
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Stevanin G.,Durr A.,Dussert C.,Penet C.,Brice A.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 12 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. Broader phenotypic traits and widespread brain hypometabolism in spinocerebellar ataxia 27;Journal of Internal Medicine;2020-03-19

2. A novel frameshift mutation in FGF14 causes an autosomal dominant episodic ataxia;neurogenetics;2015-01-08

3. Spinocerebellar ataxia type 27 (SCA27) is an uncommon cause of dominant ataxia among Chinese Han population;Neuroscience Letters;2012-06

4. Autosomal dominant cerebellar ataxias;Revue Neurologique;2011-05

5. Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds;Journal of Neurology, Neurosurgery & Psychiatry;2010-07-28

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