Calreticulin gene exon 9 frameshift mutations in patients with thrombocytosis
Jufang Chi(Center for the Study of Childhood and Adolescence), Paul Costeas(Deakin University), Andrie Mitsidou(Center for the Study of Childhood and Adolescence), Chrystalla Prokopiou(Limassol General Hospital), George S. Vassiliou(Wellcome/MRC Cambridge Stem Cell Institute), Chryso Pierides(Center for the Study of Childhood and Adolescence), Laura Koumas, Frederiki Melanthiou(Nicosia General Hospital), K Barbouti(Center for the Study of Childhood and Adolescence), K A Nicolaou(Center for the Study of Childhood and Adolescence), Menelaos Manoloukos(Center for the Study of Childhood and Adolescence)
Cited by 57
Related Papers
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
|The Lancet|2005|3.4k
A CRISPR Dropout Screen Identifies Genetic Vulnerabilities and Therapeutic Targets in Acute Myeloid Leukemia
|Cell Reports|2016|834
Molecular and functional characterization of the Salmonella invasion gene invA: homology of InvA to members of a new protein family
|Journal of Bacteriology|1992|586
Clonal dynamics of haematopoiesis across the human lifespan
|Nature|2022|505