Polyglutamine aggregation in Huntington's disease and spinocerebellar ataxia type 3: similar mechanisms in aggregate formation-Reference-Cited by-同舟云学术

Polyglutamine aggregation in Huntington's disease and spinocerebellar ataxia type 3: similar mechanisms in aggregate formation

Author:

Seidel K.¹,Siswanto S.¹,Fredrich M.¹,Bouzrou M.¹,Brunt E. R.²,van Leeuwen F. W.³,Kampinga H. H.⁴,Korf H. -W.¹,Rüb U.¹,den Dunnen W. F. A.⁵

Affiliation:

1. Dr. Senckenbergisches Chronomedizinisches Institut; Goethe University; Frankfurt/Main Germany

2. Department of Neurology; University of Groningen; Groningen The Netherlands

3. Department of Neuroscience; Maastricht University; Maastricht The Netherlands

4. Cell Biology, Radiation and Stress Cell Biology; University of Groningen; Groningen The Netherlands

5. Department of Pathology and Medical Biology; University Medical Center Groningen; University of Groningen; Groningen The Netherlands

Funder

Dr. Senckenbergische Stiftung

ADCA-Vereniging Nederland

Stiftung Hoffnung

Deutsche Huntington Hilfe

deutsche Heredo-Ataxie Gesellschaft

International Stichting Alzheimer Onderzoek

Hersenstichting Nederland grant

Publisher

Wiley

Subject

Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine

Reference54 articles.

4. Huntington's disease;Walker;Semin Neurol,2007

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