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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.
WITH INVITAE, YOU’RE PART OF THE SOLUTION
Thanks to people like you, the experience of living with genetic conditions can be understood like never before. The more health information we collect through patient surveys and uploaded medical reports, the closer we can get to helping communities find treatments that work.
The KAT6A Foundation is a patient-led organization dedicated to understanding the impacts of mutations to the KAT6A gene and to developing effective treatments for those suffering from associated conditions. Learn more about the impacts of KAT6A mutations at www.chloekat6a.org.
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.
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