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Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation

PaperCitations, authors & open-access status

Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation is a paper indexed in PICO Portal from OpenAlex.

How many citations does Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation have?

PICO Portalcitation count

Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation has 63 citations in the OpenAlex counts PICO Portal stores.

When was Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation published?

PICO Portalyear

Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation has 2013 year in the PICO Portal index.

What is the open-access status of Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation?

PICO Portaloa status

Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation has closed oa status in the PICO Portal index.

What is the DOI of Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation?

PICO Portaldoi

The DOI for Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation is on the source record.

What is the PMID of Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation?

PICO Portalpmid

The PMID for Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation is on the source record.

What is the OpenAlex record for Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation?

PICO Portalopenalex

The OpenAlex for Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation is on the source record.

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