Hereditary spastic paraplegia: gain-of-function mechanisms revealed by new transgenic mouse
Author:
Affiliation:
1. Department of Neurobiology and Anatomy
2. Department of Neurology, Drexel University College of Medicine, Queen Lane, Philadelphia, PA, USA
3. Department of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago, IL, USA
Funder
Drexel Dean’s Fellowship for Excellence in Collaborative Research Training
Tom Wahlig Foundation
National Institutes of Health
Spastic Paraplegia Foundation
ALS Hope Foundation
Craig H. Neilsen Foundation
Drexel University College of Medicine
Pennsylvania Department of Health
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/28/7/1136/28073533/ddy419.pdf
Reference78 articles.
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2. Modeling axonal defects in hereditary spastic paraplegia with human pluripotent stem cells;Denton;Front. Biol. (Beijing),2016
3. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia;Hazan;Nat. Genet.,1999
4. Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia;Fonknechten;Hum. Mol. Genet.,2000
5. Hereditary spastic paraplegia caused by mutations in the SPG4 gene;Burger;Eur. J. Hum. Genet.,2000
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