Novel CACNA1A mutation(s) associated with slow saccade velocities-Reference-Cited by-同舟云学术

Novel CACNA1A mutation(s) associated with slow saccade velocities

Published:2013-09-18 Issue:12 Volume:260 Page:3010-3014
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Kipfer Stefan,Jung Simon,Lemke Johannes R.,Kipfer-Kauer Anna,Howell Jeremy P.,Kaelin-Lang Alain,Nyffeler Thomas,Gutbrod Klemens,Abicht Angela,Müri René M.

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-013-7099-4.pdf

Reference17 articles.

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3. Kullmann DM, Hanna MG (2002) Neurological disorders caused by inherited ion-channel mutations. Lancet Neurol 1:157–166

4. Zhuchenko O, Bailey J, Bonnen P et al (1997) Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. Nat Genet 15:62–69

5. Romaniello R, Zucca C, Tonelli A et al (2010) A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation. J Neurol Neurosurg Psychiatry 81:840–843

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