B
y working together and sharing information, the KAT6A Foundation asks those with confirmed KAT6A mutations as well as individuals with mutations in any of the genes in the lysine(K) acetyl transferase (KAT) family to participate in this Patient Insights Network (PIN). We welcome patients with confirmed mutations in genes that are in the lysine(K) acetyl transferase family of genes to contribute their data and help us understand how lysine acetyl transferase function affects human development, and how we might treat the mutations in these genes.
Your participation helps us all define the disease(s) affiliated with KAT6A and associated mutations, to inform the development of therapies and treatments, and to increase our knowledge of disease progression.
