JAK2, MPL, and CALR mutations in children with essential thrombocythemia

Issue Title: Including PIH Articles on Recent advance in the diagnosis and treatment of bone marrow failure syndromes

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Bibliographic Details
Published inInternational journal of hematology Vol. 104; no. 2; pp. 266 - 267
Main Authors Sekiya, Yuko, Okuno, Yusuke, Muramatsu, Hideki, Ismael, Olfat, Kawashima, Nozomu, Narita, Atsushi, Wang, Xinan, Xu, Yinyan, Hama, Asahito, Fujisaki, Hiroyuki, Imamura, Toshihiko, Hasegawa, Daiichiro, Kosaka, Yoshiyuki, Sunami, Shosuke, Ohtsuka, Yoshitoshi, Ohga, Shouichi, Takahashi, Yoshiyuki, Kojima, Seiji, Shimada, Akira
Format Journal Article
LanguageEnglish
Published Tokyo Springer Japan 01.08.2016
Springer Nature B.V
Subjects
Adolescent
Calreticulin - genetics
Child
Child, Preschool
Hematology
Humans
Janus Kinase 2 - genetics
Letter to the Editor
Medicine
Medicine & Public Health
Mutation
Oncology
Receptors, Thrombopoietin - genetics
Thrombocythemia, Essential - genetics
Adult Cohort
Essential Thrombocythemia
Myelofibrosis
Somatic Mutation
Pediatric Patient
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Summary:Issue Title: Including PIH Articles on Recent advance in the diagnosis and treatment of bone marrow failure syndromes
Bibliography:SourceType-Other Sources-1
content type line 63
ObjectType-Correspondence-1
ISSN:0925-5710
1865-3774
DOI:10.1007/s12185-016-2022-2