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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Bibliografiske detaljer

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
Format:	Artigo
Sprog:	Inglês
Udgivet:	Taylor & Francis Group 2018-11-01
Serier:	Platelets
Fag:	inherited macrothrombocytopenia myh9 next generation sequencing platelets thrombopoietin agonists
Online adgang:	http://dx.doi.org/10.1080/09537104.2017.1356920
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