Article
Immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: association of subcellular localization with MYH9 mutations.
Laboratory investigation; a journal of technical methods and pathology - 1 Jan 2003
Kunishima Shinji, Matsushita Tadashi, Kojima Tetsuhito, Sako Masahiro, Kimura Fumihiro, Jo Eun-Kyeong, Inoue Chikako, Kamiya Tadashi, Saito Hidehiko
Abstract excerpt
The autosomal dominant macrothrombocytopenia with leukocyte inclusions, May-Hegglin anomaly, Sebastian syndrome, and Fechtner syndrome, are rare human disorders characterized by a triad of giant platelets, thrombocytopenia, and characteristic Döhle body-like cytoplasmic inclusions in granulocytes. Epstein syndrome is another autosomal dominant macrothrombocytopenia associated with Alport syndrome but without...
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