Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration-Reference-Cited by-同舟云学术

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Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration

Published:2012-05-30 Issue:24 Volume:109 Page:9611-9616
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Dehay B.,Ramirez A.,Martinez-Vicente M.,Perier C.,Canron M.-H.,Doudnikoff E.,Vital A.,Vila M.,Klein C.,Bezard E.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference36 articles.

1. Recent Advances in the Genetics of Parkinson's Disease

2. Pallido-pyramidal degeneration, supranuclear upgaze paresis and dementia: Kufor-Rakeb syndrome

3. Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

4. ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease

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