A Trp33Arg Mutation at Exon 1 of theMYH9Gene in a Korean Patient with May-Hegglin Anomaly

Identification of three in-frame deletion mutations inMYH9disorders suggesting an important hot spot for small rearrangements inMYH9exon 24

(2009) Koji Miyazaki et al.   EUROPEAN JOURNAL OF HAEMATOLOGY

MYH9-Related Platelet Disorders

(2009) Karina Althaus et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS

Differential expression of wild-type and mutant NMMHC-IIA polypeptides in blood cells suggests cell-specific regulation mechanisms in MYH9 disorders

(2008) S. Kunishima et al.   BLOOD

Accumulation ofMYH9mRNA at leukocyte inclusion bodies inMYH9disorders

(2008) Shinji Kunishima et al.   EUROPEAN JOURNAL OF HAEMATOLOGY

Identification and characterization of the first large deletion of theMYH9gene associated withMYH9disorders

(2008) Shinji Kunishima et al.   EUROPEAN JOURNAL OF HAEMATOLOGY

Identification of the firstin cismutations inMYH9disorder

(2008) Yuji Miyajima et al.   EUROPEAN JOURNAL OF HAEMATOLOGY

Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history ofMYH9-related disease

(2007) Alessandro Pecci et al.   HUMAN MUTATION