A new variant of the ATP13A2 gene in Chinese patients with early-onset parkinsonism

Parkinson's disease (PD) is the second most common neurodegenerative disorder characterized by a selective loss of nigrostriatal dopaminergic neurons. Clinical manifestations of this complex disease include resting tremor, bradykinesia, postural instability, gait difficulty and rigidity. Approximate...

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Veröffentlicht in:Chinese medical journal 2009-12, Vol.122 (24), p.3082-3085
Hauptverfasser: Wang, Lei, Guo, Ji-Feng, Nie, Li-Luo, Zhang, Hai-Nan, Shen, Lu, Jiang, Hong, Pan, Qian, Xia, Kun, Tang, Bei-Sha, Yan, Xin-Xiang
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Sprache:eng
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Zusammenfassung:Parkinson's disease (PD) is the second most common neurodegenerative disorder characterized by a selective loss of nigrostriatal dopaminergic neurons. Clinical manifestations of this complex disease include resting tremor, bradykinesia, postural instability, gait difficulty and rigidity. Approximately 5%-10% of patients have genetic factors, yet etiology of PD remains unclear. Genetic deficits, environmental exposure, oxidative stress, mitochondrial dysfunction,
ISSN:0366-6999
2542-5641
DOI:10.3760/cma.j.issn.0366-6999.2009.24.032