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Parkinson disease penetrance in patients with Gaucher disease and in glucocerebrosidase mutation carriers

✍ Scribed by Dinur, Tama; Quinn, Timothy; Sakanaka, Karina; Levy, Oren; Marder, Karen S.; Waters, Cheryl; Fahn, Stanley; Dorovski, Tsvyatko; Pauciulo, Michael; Nichols, William; Rana, Huma Q.; Balwani, Manisha; Bier, Louise; Elstein, Deborah; Zimran, Ari; Alcalay, Roy N.

Book ID
122151405
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
73 KB
Volume
111
Category
Article
ISSN
1096-7192

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## Communicated by Mark Paalman Gaucher disease, the most common lysosomal storage disorder, results from the inherited deficiency of the enzyme glucocerebrosidase. Three clinical types are recognized: type 1, nonneuronopathic; type 2, acute neuronopathic; and type 3, subacute neuronopathic. Type 2