Author:
Hellenbroich Y.,Bernard V.,Zühlke C.
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Reference13 articles.
1. Flanigan K, Gardner K, Alderson K, Galster B, Otterud B, Leppert MF, Kaplan C, Ptacek LJ (1996) Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22. 1. Am J Hum Genet 59:392–399
2. Hellenbroich Y, Bubel S, Pawlack H, Opitz S, Vieregge P, Schwinger E, Zuhlke C (2003) Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region. J Neurol 250:668–671
3. Hellenbroich Y, Pawlack H, Rub U, Schwinger E, Zuhlke C (2005) Spinocerebellar ataxia type 4. Investigation of 34 candidate genes. J Neurol 252:1472–1475
4. Hellenbroich Y, Gierga K, Reusche E, Schwinger E, Deller T, de Vos RA, Zuhlke C, Rub U (2006) Spinocerebellar ataxia type 4 (SCA4): Initial pathoanatomical study reveals widespread cerebellar and brainstem degeneration. J Neural Transm 113:829–843
5. Nagaoka U, Takashima M, Ishikawa K, Yoshizawa K, Yoshizawa T, Ishikawa M, Yamawaki T, Shoji S, Mizusawa H (2000) A gene on SCA4 locus causes dominantly inherited pure cerebellar ataxia. Neurology 54:1971–1975
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