Fig. 1From: Immunological repertoire linked to PSTPIP1-associated myeloid-related inflammatory (PAMI) syndromeGenetic sequencing and baseline laboratory analysis of patients harboring the E250K mutation in gene PSTIPIP1. A) Family pedigree and electropherograms demonstrating an autosomal dominant pattern of inheritance. B) Baseline laboratory analysis of the index patient and her mother, evidencing anemia, neutropenia in both patients and thrombocytopenia in the index patientBack to article page