Nonfamilial, MPL S505N-Mutated Essential Thrombocythaemia
Mutations of MPL are present in a significant proportion of patients with the myeloproliferative neoplasms (MPN), primary myelofibrosis (PMF), and essential thrombocythaemia (ET). The most frequent of these mutations, W515L and W515K, occur in exon 10 of MPL, which encodes the receptor for thrombopo...
Saved in:
Main Authors: | Ruth Morrell, Stephen E. Langabeer, Liam Smyth, Meegahage Perera, Gerard Crotty |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2013-01-01
|
Series: | Case Reports in Hematology |
Online Access: | http://dx.doi.org/10.1155/2013/729327 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Prefibrotic Myelofibrosis Presenting with Multiple Cerebral Embolic Infarcts and the Rare MPL W515S Mutation
by: Stephen E. Langabeer, et al.
Published: (2020-01-01) -
Nonfamilial Juvenile Polyposis Syndrome with Exon 5 Novel Mutation in SMAD 4 Gene
by: Amna Ahmed, et al.
Published: (2017-01-01) -
Corrigendum to “Nonfamilial Juvenile Polyposis Syndrome with Exon 5 Novel Mutation in SMAD 4 Gene”
by: Amna Ahmed, et al.
Published: (2017-01-01) -
A Rare Co-Occurrence of Triple Mutations in JAK2, CALR, and MPL in the Same Patient with Myelofibrosis
by: Sherine J. Thomas, et al.
Published: (2022-01-01) -
Acute Lymphoblastic Leukemia Arising in CALR Mutated Essential Thrombocythemia
by: Stephen E. Langabeer, et al.
Published: (2016-01-01)