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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 PICO Portal from OpenAlex.

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

PICO Portalcitation count

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

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

PICO Portalyear

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

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

PICO Portaloa status

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

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

PICO Portaldoi

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?

PICO Portalpmid

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?

PICO Portalopenalex

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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