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Ocular Phenotype Associated with DYRK1A Variants

January 20, 2021 Amy Clugston

Full Article

In DYRK1A Patient Research Tags Present Day - 2015
← Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorderGenetic diagnosis of infantile-onset epilepsy in the clinic: Application of whole-exome sequencing following epilepsy gene panel testing →

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