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A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease
PaperCitations, authors & open-access status
A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease is a paper indexed in ScholarIQ from OpenAlex.
How many citations does A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease have?
ScholarIQcitation count
A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease has 115 citations in the OpenAlex counts ScholarIQ stores.
When was A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease published?
ScholarIQyear
A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease has 2021 year in the ScholarIQ index.
What is the open-access status of A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease?
ScholarIQoa status
A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease has hybrid oa status in the ScholarIQ index.
What is the DOI of A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease?
ScholarIQdoi
The DOI for A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease is on the source record.
What is the PMID of A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease?
ScholarIQpmid
The PMID for A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease is on the source record.
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ScholarIQopenalex
The OpenAlex for A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease is on the source record.