Impaired mitochondrial dynamics underlie axonal defects in hereditary spastic paraplegias-Reference-Cited by-同舟云学术

Impaired mitochondrial dynamics underlie axonal defects in hereditary spastic paraplegias

Published:2018-05-02 Issue:14 Volume:27 Page:2517-2530
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Denton Kyle¹,Mou Yongchao²³,Xu Chong-Chong²³,Shah Dhruvi²,Chang Jaerak⁴⁵,Blackstone Craig⁴,Li Xue-Jun²³

Affiliation:

1. Department of Neuroscience, University of Connecticut Health Center, Farmington, CT, USA

2. Department of Biomedical Sciences, University of Illinois College of Medicine at Rockford, Rockford, IL, USA

3. Department of Bioengineering, University of Illinois at Chicago, Chicago, IL, USA

4. Cell Biology Section, Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA

5. Departments of Biomedical Science, Brain Science, and Neuroscience Graduate Program, Ajou University School of Medicine, Suwon, Korea

Funder

National Institutes of Health

Blazer Foundation

Movement Disorder Foundation

NINDS

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/27/14/2517/25099026/ddy156.pdf

Reference66 articles.

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2. Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders;Novarino;Science,2014

3. SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum;Goizet;Neurology,2009

4. Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48;Pensato;Brain,2014

5. Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome;Hanein;Am. J. Hum. Genet,2008

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