1. Syndromic congenital myelofibrosis associated with a loss-of-function variant in RBSN
- Author
-
Richard A. Gibbs, Lorraine Potocki, Andrea N. Marcogliese, Silvia Corvera, Svetlana A. Yatsenko, Shay Ben-Shachar, Gladys Zapata, Luis M. Franco, Donna M. Muzny, Oleg A Shchelochkov, Derek Einhaus, Richard A. Lewis, Daryl A. Scott, Charles Searby, Pilar L. Magoulas, M. Tarek Elghetany, Matthew N. Bainbridge, Manasi Gadkari, Paula P. Hernández, and Alison A. Bertuch
- Subjects
0301 basic medicine ,business.industry ,Immunology ,Cell Biology ,Hematology ,Endosomes ,Bioinformatics ,medicine.disease ,Biochemistry ,03 medical and health sciences ,Protein Transport ,030104 developmental biology ,0302 clinical medicine ,Text mining ,Cell Movement ,Primary Myelofibrosis ,030220 oncology & carcinogenesis ,Medicine ,Humans ,business ,Myelofibrosis ,Letter to Blood ,Loss function - Abstract
Publisher's Note: There is a Blood Commentary on this article in this issue.
- Published
- 2018