PICO Portalanswers from OpenAlex
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 PICO Portal from OpenAlex.
How many citations does A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease have?
PICO Portalcitation count
A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease has 115 citations in the OpenAlex counts PICO Portal stores.
When was A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease published?
PICO Portalyear
A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease has 2021 year in the PICO Portal index.
What is the open-access status of A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease?
PICO Portaloa status
A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease has hybrid oa status in the PICO Portal index.
What is the DOI of A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease?
PICO Portaldoi
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?
PICO Portalpmid
The PMID for A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease is on the source record.
What is the OpenAlex record for A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease?
PICO Portalopenalex
The OpenAlex for A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease is on the source record.