Spinocerebellar ataxia type 11-Reference-Cited by-同舟云学术

Spinocerebellar ataxia type 11

Published:2012 Issue: Volume: Page:521-534
ISSN:0072-9752
Container-title:Handbook of Clinical Neurology
language:
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Author:

Giunti P.,Houlden H.,Gardner-Thorpe C.,Worth P.F.,Johnson J.,Hilton D.A.,Revesz T.,Davis M.B.,Wood N.W.

Publisher

Elsevier

Reference39 articles.

1. Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval;Allamand;Am J Hum Genet,1995

2. Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds;Bauer;J Neurol Neurosurg Psychiatry,2010

3. Oculomotor phenotypes in autosomal dominant ataxias;Buttner;Arch Neurol,1998

4. A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene;Chiannilkulchai;Hum Mol Genet,1995

5. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23;Chung;Brain,2003

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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. Clinical Characteristics and Possible Drug Targets in Autosomal Dominant Spinocerebellar Ataxias;CNS & Neurological Disorders - Drug Targets;2019-07-17

4. The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerability;Journal of Neurology, Neurosurgery & Psychiatry;2014-08-18