Compound heterozygous mutations in PARK2 causing early-onset Parkinson disease: A case report

RATIONALE: Parkinson disease (PD) is a complex neurodegenerative movement disorder characterized by resting tremor, muscular rigidity, bradykinesia, and so on. Genetics has been regarded as an important role in the development of PD. PARK2, an autosomal recessive gene, is the most common one referri...

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Detalles Bibliográficos
Autores principales: Fang, Yu-Qing, Mao, Fei, Zhu, Mei-Jia, Li, Xiu-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6380659/
https://www.ncbi.nlm.nih.gov/pubmed/30702579
http://dx.doi.org/10.1097/MD.0000000000014228

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6380659/
https://www.ncbi.nlm.nih.gov/pubmed/30702579
http://dx.doi.org/10.1097/MD.0000000000014228

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