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 ScholarIQ from OpenAlex.

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Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations has 499 citations in the OpenAlex counts ScholarIQ 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 ScholarIQ index.

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

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