An unusual long-term outcome of a child with primary myelofibrosis harboring a JAK2 mutation.

Maia, Raquel Ciuvalschi

An unusual long-term outcome of a child with primary myelofibrosis harboring a JAK2 mutation. [electronic resource] - Blood cells, molecules & diseases Dec 2015 - 347-50 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1096-0961

10.1016/j.bcmd.2015.07.013 doi


Female
Follow-Up Studies
Humans
Infant
Janus Kinase 2--genetics
Mutation
Phenotype
Primary Myelofibrosis--diagnosis