Article
Clinical and laboratory characteristics in congenital ANKRD26 mutation-associated thrombocytopenia: A detailed phenotypic study of a family.
Platelets - 1 Nov 2016
Perez Botero Juliana, Chen Dong, He Rong, Viswanatha David S, Majerus Julie A, Coon Lea M, Nguyen Phuong L, Reichard Karen K, Oliveira Jennifer L, Tefferi Ayalew, Gangat Naseema, Pruthi Rajiv K, Patnaik Mrinal M
Abstract excerpt
The clinical and laboratory characteristics of patients with non-syndromic, autosomal dominant thrombocytopenia secondary to germ line ANKRD26 mutations appear to be heterogeneous. Except for a targeted molecular genotyping approach, there is no distinct clinical or laboratory phenotype that has been specifically associated with this particular gene mutation. Such heterogeneity could be due to variations in...
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