相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。ACTN1 Mutations Cause Congenital Macrothrombocytopenia
Shinji Kunishima et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Familial cases with MYH9 disorders caused by MYH9 S96L mutation
Shizuko Murayama et al.
PEDIATRICS INTERNATIONAL (2013)
Frequent pathway mutations of splicing machinery in myelodysplasia
Kenichi Yoshida et al.
NATURE (2011)
Heavy chain myosin 9-related disease (MYH9-RD): Neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder
Anna Savoia et al.
THROMBOSIS AND HAEMOSTASIS (2010)
Mutation of the β1-tubulin gene associated with congenital macrothrombocytopenia affecting microtubule assembly
Shinji Kunishima et al.
BLOOD (2009)
Immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: Association of subcellular localization with MYH9 mutations
S Kunishima et al.
LABORATORY INVESTIGATION (2003)
Immunocytochemistry for the heavy chain of the non-muscle myosin IIA as a diagnostic tool for MYH9-related disorders
A Pecci et al.
BRITISH JOURNAL OF HAEMATOLOGY (2002)
Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome)
S Kunishima et al.
BLOOD (2001)
Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly
MJ Kelley et al.
NATURE GENETICS (2000)
分享论文
