Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations is a paper indexed in PICO Portal from OpenAlex.

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Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations has 499 citations in the OpenAlex counts PICO Portal stores.

When was Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations published?

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations has 2010 year in the PICO Portal index.

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Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations has green oa status in the PICO Portal index.

What is the DOI of Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations?

The DOI for Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations is on the source record.

What is the PMID of Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations?

The PMID for Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations is on the source record.

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The OpenAlex for Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations is on the source record.