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Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene

PaperCitations, authors & open-access status

Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene is a paper indexed in PICO Portal from OpenAlex.

How many citations does Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene have?

PICO Portalcitation count

Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene has 127 citations in the OpenAlex counts PICO Portal stores.

When was Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene published?

PICO Portalyear

Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene has 2012 year in the PICO Portal index.

What is the open-access status of Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene?

PICO Portaloa status

Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene has closed oa status in the PICO Portal index.

What is the DOI of Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene?

PICO Portaldoi

The DOI for Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene is on the source record.

What is the PMID of Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene?

PICO Portalpmid

The PMID for Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene is on the source record.

What is the OpenAlex record for Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene?

PICO Portalopenalex

The OpenAlex for Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene is on the source record.

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