Clinical characteristics and platelet phenotype in a family with RUNX1 mutated thrombocytopenia. Leuk Lymphoma 2017 Aug;58(8):1963-1967
Date
12/10/2016Pubmed ID
27931139DOI
10.1080/10428194.2016.1265118Scopus ID
2-s2.0-85003977139 (requires institutional sign-in at Scopus site) 10 CitationsAuthor List
Perez Botero J, Chen D, Cousin MA, Majerus JA, Coon LM, Kruisselbrink TM, Klee EW, Lazaridis KN, Pruthi RK, Patnaik MMMESH terms used to index this publication - Major topics in bold
AdultBlood Platelets
Core Binding Factor Alpha 2 Subunit
Female
Haploinsufficiency
Humans
Immunophenotyping
Mutation
Nonsense Mediated mRNA Decay
Pedigree
Phenotype
RNA Splicing
Symptom Assessment
Thrombocytopenia
