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QuickView for KAT6B;jsessionid=3AF6582FCE9B76A30AFDE2755BDF2B68 (gene)
Most Relevant Literature
- Clinical heterogeneity of polish patients with KAT6B-related disorder.
- Increasing histone acetylation improves sociability and restores learning and memory in KAT6B-haploi…
- De novo KAT6B mutation causes Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome in an Iran…
- Clinical features and underlying mechanisms of KAT6B disease in a Chinese boy.
- DNA methylation episignatures are sensitive and specific biomarkers for detection of patients with K…
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