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Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

PaperCitations, authors & open-access status

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction is a paper indexed in PICO Portal from OpenAlex.

How many citations does Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction have?

PICO Portalcitation count

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction has 57 citations in the OpenAlex counts PICO Portal stores.

When was Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction published?

PICO Portalyear

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction has 2021 year in the PICO Portal index.

What is the open-access status of Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction?

PICO Portaloa status

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction has bronze oa status in the PICO Portal index.

What is the DOI of Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction?

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The DOI for Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction is on the source record.

What is the PMID of Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction?

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The PMID for Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction is on the source record.

What is the OpenAlex record for Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction?

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The OpenAlex for Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction is on the source record.

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