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A novel de novo heterozygous DYRK1A mutation causes complete loss of DYRK1A function and developmental delay

June 17, 2020 Amy Clugston

Full Article

In DYRK1A Patient Research Tags Present Day - 2015
← Neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and brain size in Xenopus embryos Impact of DYRK1A Haploinsufficiency on Facial Morphology using Three-Dimensional Morphometric Analysis →

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