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The contribution of Niemann-Pick SMPD1 mutations to Parkinson disease in Ashkenazi Jews
E. Dagan
, I. Schlesinger
, M. Ayoub
, A. Mory
, M. Nassar
, A. Kurolap
, J. Peretz-Aharon
, R. Gershoni-Baruch
Department of Nursing
Research output
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Contribution to journal
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peer-review
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Keyphrases
Ashkenazi Jews
100%
Parkinson's Disease
100%
Sphingomyelin Phosphodiesterase 1
100%
Niemann-Pick
100%
Ashkenazi
50%
Leucine-rich Repeat Kinase 2 (LRRK2)
37%
Parkinson Patients
37%
Founder mutation
37%
G2019S mutation
25%
Risk Factors
12%
Phenotypic Expression
12%
Clinical Characteristics
12%
Neurobehavior
12%
Neurological Examination
12%
Unified Parkinson's Disease Rating Scale (UPDRS)
12%
Disruptive mutation
12%
Lysosomal Storage Disease
12%
Biochemistry, Genetics and Molecular Biology
Sphingomyelin Phosphodiesterase 1
100%
LRRK2
37%
Lysosomal Storage Disease
12%