RUNX1

Familial platelet disorder with myeloid malignancies (FPDMM)

1 article(s) in the watch · Constitutional genetics

Curated publications

Functional analysis of germline RUNX1 variants identified in individuals with suspected familial platelet disorder

Familial platelet disorder with myeloid malignancies (FPDMM)

Automatic aggregation page — a clinical introduction may be added.