De novo apparent loss-of-function mutations in PRR12 in three patients with intellectual disability and iris abnormalities

Overview of attention for article published in Human Genetics, March 2018

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Shedding a Light on Dark Genes: A Comparative Expression Study of PRR12 Orthologues during Zebrafish Development

Article in Genes (April 2024)

Co-Essentiality Analysis Identifies PRR12 as a Regulator of Cohesin and Genome Integrity

Preprint in bioRxiv (March 2024)

Genetic network analysis indicate that individuals affected by neurodevelopmental conditions have genetic variations associated with ophthalmologic alterations: A critical review of literature

Article in Gene (February 2024)

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