Clinical Characterization of Genetically Diagnosed Cases of Spinocerebellar Ataxia Type 12 from India-Reference-Cited by-同舟云学术

Clinical Characterization of Genetically Diagnosed Cases of Spinocerebellar Ataxia Type 12 from India

Published:2017-11-01 Issue:1 Volume:5 Page:39-46
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Mov Disord Clin Pract

Author:

Choudhury Supriyo¹,Chatterjee Sayan¹,Chatterjee Koustav¹,Banerjee Rebecca¹,Humby Jonathan²,Mondal Banashree¹,Anand Sidharth S.¹,Shubham Shantanu¹,Kumar Hrishikesh¹

Affiliation:

1. Department of Neurology; Institute of Neurosciences; Kolkata India

2. Institute of Neuroscience; Newcastle University; Newcastle upon Tyne United Kingdom

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mdc3.12551/fullpdf

Reference44 articles.

1. Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12;Holmes;Nat Genet,1999

2. Margolis RL Holmes SE Srivastava AK Mukherji Mitali Sinha KK Adam MP Ardinger HH Pagon RA

3. SCA-12: tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion;O'Hearn;Neurology,2001

4. The SCA12 mutation as a rare cause of spinocerebellar ataxia;Cholfin;Arch Neurol,2001

5. SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family;Fujigasaki;Ann Neurol,2001

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