Ataxia-telangiectasia: A review of movement disorders, clinical features, and genotype correlations-Reference-Cited by-同舟云学术

Ataxia-telangiectasia: A review of movement disorders, clinical features, and genotype correlations

Published:2018-02-13 Issue:8 Volume:33 Page:1238-1247
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Levy Ariel¹²³,Lang Anthony E.¹²^ORCID

Affiliation:

1. Edmond J Safra Program in Parkinson's Disease, Toronto Western Hospital; Toronto Ontario Canada

2. Morton and Gloria Shulman Movement Disorders Clinic; Toronto Ontario Canada

3. Department of Neuroscience, Faculty of Medicine; Université de Montréal, Montreal; Quebec Canada

Funder

Parkinson Canada Clinical Fellowship Award

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.27319/fullpdf

Reference49 articles.

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2. Ataxia-telangiectasia; a familial syndrome of progressive cerebellar ataxia, oculocutaneous telangiectasia and frequent pulmonary infection;Boder;Pediatrics,1958

3. A single ataxia telangiectasia gene with a product similar to PI-3 kinase;Savitsky;Science,1995

4. Ataxia telangiectasia;Crawford;Semin Pediatr Neurol,1998

5. Presence of ATM protein and residual kinase activity correlates with the phenotype in ataxia-telangiectasia: a genotype-phenotype study;Verhagen;Hum Mutat,2012

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