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Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene

PaperCitations, authors & open-access status

Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene have?

ScholarIQcitation count

Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene has 32 citations in the OpenAlex counts ScholarIQ stores.

When was Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene published?

ScholarIQyear

Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene has 2016 year in the ScholarIQ index.

What is the open-access status of Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene?

ScholarIQoa status

Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene has closed oa status in the ScholarIQ index.

What is the DOI of Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene?

ScholarIQdoi

The DOI for Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene is on the source record.

What is the PMID of Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene?

ScholarIQpmid

The PMID for Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene is on the source record.

What is the OpenAlex record for Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene?

ScholarIQopenalex

The OpenAlex for Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene is on the source record.

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