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Disruption of the histone acetyltransferase MYST4 leads to a Noonan syndrome–like phenotype and hyperactivated MAPK signaling in humans and mice

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Academic year: 2020

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Figure

Figure 1Phenotype and genetic studies in the patient with MYST4 haploinsufficiency at age 6 years
Figure 2Structure and histone acetylation of MYST4. (
Figure 3Effect of different
Figure 4Qkf mutant mice deficient in Myst4.
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