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Age‐Related Parkinsonian Signs in Microdeletion 22q11.2
BACKGROUND: The recurrent hemizygous 22q11.2 deletion associated with 22q11.2 deletion syndrome has been identified as a genetic risk factor for early‐onset PD. However, little is known about early motor signs in this condition. OBJECTIVES: We examined the presence, severity and possible factors ass...
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| 出版年: | Mov Disord |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley & Sons, Inc.
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7497092/ https://ncbi.nlm.nih.gov/pubmed/32386091 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.28080 |
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