Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: A novel entity?

Author:

Wictorin Klas,Brådvik Björn,Nilsson Karin,Soller Maria,van Westen Danielle,Bynke Gunnel,Bauer Peter,Schöls Ludger,Puschmann AndreasORCID

Funder

EU

Publisher

Elsevier BV

Subject

Neurology (clinical),Geriatrics and Gerontology,Neurology

Reference30 articles.

1. Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?;Schols;Ann Neurol,1997

2. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis;Schols;Lancet Neurol,2004

3. Ataxias;Klockgether;Parkinsonism Relat Disord,2007

4. Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics;Whaley;Orphanet J Rare Dis,2011

5. Monogenic Parkinson's disease and parkinsonism: clinical phenotypes and frequencies of known mutations;Puschmann;Parkinsonism Relat Disord,2013

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