authors
- Lu, Wei
- Lenardo, Michael
- Karuppagounder, Senthilkumar S
- Springer, Danielle A
- Allen, Michele D
- Zheng, Lixin
- Chao, Brittany
- Zhang, Yan
- Dawson, Valina L
- Ted M. Dawson, MD, PhD
Genetic deficiency of the mitochondrial protein PGAM5 causes a Parkinson's-like movement disorder.
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Overview
publication date
- January 1, 2014
published in
- Nature communications Journal
has subject area
- Animals
- Behavior, Animal
- Disease Models, Animal
- Dopamine
- Dopaminergic Neurons
- Female
- Fibroblasts
- Gene Expression Regulation
- Mice
- Mice, Knockout
- Mitochondria
- Mitochondrial Proteins
- Mitophagy
- Motor Activity
- Parkinson Disease, Secondary
- Phosphoprotein Phosphatases
- Phosphoric Monoester Hydrolases
- Protein Kinases
- RNA, Small Interfering
- Signal Transduction