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The RUNX1 Research Program aims to increase awareness of RUNX1-FPD both in the general public and medical communities, and to provide grants for groundbreaking research projects in the hope of finding a cure. Please spread the word about us and that inherited blood cancers do exist.
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Breaking New Ground
The NIH has just initiated the first-ever longitudinal natural history study of RUNX1-FPD patients, with the aim of better understanding the clinical features of the disease, how these may relate to the different germline mutations and why some patients progress to blood cancer and others do not. This is a groundbreaking study and essential in our effort to find a cure.