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Diagnosis and treatment of MYH9-RD in an Australasian cohort with thrombocytopenia

MYH9-related disorders (MYH9-RDs) caused by mutation of the MYH9 gene which encodes non-muscle myosin heavy-chain-IIA (NMMHC-IIA), an important motor protein in hemopoietic cells, are the most commonly encountered cause of inherited macrothrombocytopenia. Despite distinguishing features including an...

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Principais autores: David J. Rabbolini, Yenna Chun, Maya Latimer, Shinji Kunishima, Kathleen Fixter, Bhavia Valecha, Peter Tan, Lee Ping Chew, Benjamin T. Kile, Rachel Burt, Kottayam Radhakrishnan, Robert Bird, Paul Ockelford, Sara Gabrielli, Qiang Chen, William S. Stevenson, Christopher M. Ward, Marie-Christine Morel-Kopp
Formato: Artigo
Idioma:Inglês
Publicado: Taylor & Francis Group 2018-11-01
Series:Platelets
Assuntos:
inherited macrothrombocytopenia
myh9
next generation sequencing
platelets
thrombopoietin agonists
Acceso en liña:http://dx.doi.org/10.1080/09537104.2017.1356920
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