Condition: BLEEDING DISORDER, PLATELET-TYPE, 20


rs757188030 in SLFN14 gene and BLEEDING DISORDER, PLATELET-TYPE, 20 PMID 26280575 2015 SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects.

PMID 26769223 2016 SLFN14-related thrombocytopenia: identification within a large series of patients with inherited thrombocytopenia.