MYH9 disorder: Identification and a novel mutation in patients with macrothrombocytopenia

MYH9 disorder: Identification and a novel mutation in patients with macrothrombocytopenia

The diagnosis of MYH9 disorder is guided by recognizing granulocyte Döhle body-like inclusion bodies and large/giant platelets in the peripheral blood smear. Immunofluorescence study of nonmuscle myosin heavy chain IIA is a sensitive screening method for diagnosis of MYH9 disorder. The diagnosis can...

Full description

Saved in:
Bibliographic Details
Main Authors: Rungrote Natesirinilkul, Darintr Sosothikul, Patcharee Komwilaisak, Bunchoo Pongtanakul, Nattee Narkbunnum, Najwa Yudhasompop, Pimsiri Mekjarusgool, Pimjai Niparuck, Kochawan Boonyawat, Shinji Kunishima, Nongnuch Sirachainan, Somjai Kanjanapongkul, Thirachit Chotsampancharoen, Chanchai Trivaree, Siranee Wongruangsri, Pacharapan Surapolchai, Sumonmaln Klamchuen, Saranya Busakornruangrat, Kittima Kanchanakamhaeng, Nattaporntira Phalakornkul
Other Authors: Siriraj Hospital
Format: Article
Published: 2022
Subjects:
Medicine
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/78048
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Mahidol University

Internet

https://repository.li.mahidol.ac.th/handle/123456789/78048

Similar Items