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LRRK2, GBA and SMPD1 Founder Mutations and Parkinson's Disease in Ashkenazi Jews
Efrat Dagan
, Ilana Schlesinger
, Alina Kurolap
, Mareemar Ayoub
, Maria Nassar
, Judith Peretz-Aharon
, Ruth Gershoni-Baruch
Department of Nursing
Research output
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Contribution to journal
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Article
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peer-review
Overview
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Keyphrases
Ashkenazi Jews
100%
Parkinson's Disease
100%
Leucine-rich Repeat Kinase 2 (LRRK2)
100%
Founder mutation
100%
SMPD1
100%
Ashkenazi
75%
Non-carriers
75%
Parkinson Patients
75%
Clinical Characteristics
50%
Age at Diagnosis
50%
Mutation Carriers
50%
Patient-specific
25%
Homozygote
25%
Disease Groups
25%
LRRK2 Gene
25%
Statistical Significance
25%
Informed Consent
25%
GBA Gene
25%
Clinical Manifestations
25%
Carrier Status
25%
Bonferroni
25%
SMPD1 Gene
25%
Number of Groups
25%
GBA mutations
25%
Working Diagnosis
25%
Causative Genes
25%
Biochemistry, Genetics and Molecular Biology
LRRK2
100%
Homozygote
20%
Carrier Status
20%