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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Bibliografische gegevens
Gepubliceerd in:Mov Disord
Hoofdauteurs: Boot, Erik, Mentzel, Thierry Q., Palmer, Lisa D., van Harten, Peter N., Marras, Connie, Lang, Anthony E., Bassett, Anne S.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: John Wiley & Sons, Inc. 2020
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Regular Issue Articles
Online toegang: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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