Autosomal dominant gain-of-function mutations in LCP1 cause syndromiceneutropenia and immunodeficiency-

To further evaluate the impact of LCP1 dysfunction on hematopoiesis, we performed single-cell RNA sequencing (scRNA-seq) for bone marrow cells from patients and two matched healthy controls. Total 39, 028 cells were included in the sequential analysis after quality control. Overall design: Bone marrow cells were collected for 10X Chromium scRNA-seq.