Hereditary spastic paraplegia type 8: Neuropathological findings-Reference-Cited by-同舟云学术

Hereditary spastic paraplegia type 8: Neuropathological findings

Published:2018-03 Issue:2 Volume:28 Page:292-294
ISSN:1015-6305
Container-title:Brain Pathology
language:en
Short-container-title:Brain Pathology

Author:

Pehrson Caroline¹,Hertz Jens Michael²³,Wirenfeldt Martin¹²,Stenager Egon⁴,Wermuth Lene⁵,Winther Kristensen Bjarne¹²

Affiliation:

1. Department of Pathology; Odense University Hospital; Odense Denmark

2. Institute of Clinical Research; University of Southern Denmark; Odense Denmark

3. Department of Clinical Genetics; Odense University Hospital; Odense Denmark

4. MS-Clinic of Southern Jutland (Sønderborg, Esbjerg, Kolding), Department of Neurology, Sygehus Sønderjylland; Denmark and Institute of Regional Research, University of Southern Denmark; Denmark

5. Department of Neurology; Odense University Hospital; Odense Denmark

Publisher

Wiley

Subject

Clinical Neurology,Pathology and Forensic Medicine,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bpa.12494/fullpdf

Reference13 articles.

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2. Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegia;Bettencourt;Clin Genet,2014

3. Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases;Clemen;Brain,2010

4. Hereditary spastic paraplegia caused by a mutation in the VCP gene;Bot;Brain,2012

5. Pure adult-onset Spastic Paraplegia caused by a novel mutation in the KIAA0196 (SPG8) gene;Bot;J Neurol,2013

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