inherited thrombocytopeniaResearch
A study identifies a biallelic ITGA10 variant as a potential cause of inherited thrombocytopenia through whole-exome sequencing. This discovery adds to the understanding of genetic factors influencing platelet disorders.
biallelic itga10 variant as a candidate for inherited thrombocytopenia insights from a whole exome sequencing cohort
Original title: “A Biallelic ITGA10 Variant as a Candidate for Inherited Thrombocytopenia: Insights From a Whole-Exome Sequencing Cohort.”