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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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| Publicado no: | Medicine (Baltimore) |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Health
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6380659/ https://ncbi.nlm.nih.gov/pubmed/30702579 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000014228 |
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