Data from: Peripheral synucleinopathy in a DJ1 patient with Parkinson disease, cataracts, and hearing loss

Whereas Parkinson disease (PD) is usually sporadic, PD with onset under 50 years old can be associated with genetic abnormalities, including rare biallelic mutations in the DJ1 gene (PARK7).1 The DJ1 phenotype is incompletely described and has been presumed to be similar to the Parkin (PARK2) phenot...

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Bibliographische Detailangaben

Hauptverfasser:	Narendra, Derek P., Isonaka, Risa, Nguyen, Diana, Schindler, Alice B., Kokkinis, Angela D., Ehrlich, Debra, Bardakjian, Tanya M., Goldstein, David S., Liang, Tsao-Wei, Gonzalez-Alegre, Pedro
Format:	Dataset
Sprache:	eng
Schlagworte:	Movement disorders Neuro-ophthalmology Parkin Parkinson's disease/Parkinsonism synuclein
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