Abstract
We describe the clinical characteristics of a Swedish family with autosomal dominant cerebellar ataxia, sensory and autonomic neuropathy, additional neurological features and unknown genetic cause.
Original language | English |
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Pages (from-to) | 748-754 |
Journal | Parkinsonism & Related Disorders |
Volume | 20 |
Issue number | 7 |
DOIs | |
Publication status | Published - 2014 |
Bibliographical note
The information about affiliations in this record was updated in December 2015.The record was previously connected to the following departments: Neurology, Lund (013027000), Ophthalmology (Lund) (013043000), Diagnostic Radiology, (Lund) (013038000), Division of Clinical Genetics (013022003), Department of Psychogeriatrics (013304000)
Subject classification (UKÄ)
- Neurology