المؤلفون: Alcalay, RN, Wolf, P, Chiang, MSR, Helesicova, K, Zhang, XK, Merchant, K, Hutten, SJ, Scherzer, C, Caspell-Garcia, C, Blauwendraat, C, Foroud, T, Nudelman, K, Gan-Or, Z, Simuni, T, Chahine, LM, Levy, O, Zheng, D, Li, G, Sardi, SP

المساهمون: Michael J Fox Foundation

المصدر: 1830 ; 1816

مصطلحات موضوعية: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences, Neurosciences & Neurology, LYSOSOMAL STORAGE DISORDERS, DISEASE, MUTATIONS, PERFORMANCE, DEMENTIA, Adult, Disease Progression, Female, Genotype, Glucosylceramidase, Heterozygote, Humans, Male, Mental Status and Dementia Tests, Middle Aged, Mutation, Parkinson Disease, Phenotype, Parkinson’s Progression Markers Initiative, 1103 Clinical Sciences

Relation: Annals of Clinical and Translational Neurology; http://hdl.handle.net/10044/1/93529; WBCN_P88063

الاتاحة: http://hdl.handle.net/10044/1/93529
https://doi.org/10.1002/acn3.51164