Granulocyte whole exome sequencing and endothelial JAK2V617F in patients with JAK2V617F positive Budd-Chiari Syndrome without myeloproliferative neoplasm.

Authors :: Helman R
Pereira WO
Marti LC
Campregher PV
Puga RD
Hamerschlak N
Chiattone CS
Santos FPS
Source :: British journal of haematology [Br J Haematol] 2018 Feb; Vol. 180 (3), pp. 443-445. Date of Electronic Publication: 2016 Sep 21.
Publication Year :: 2018

Subjects :: Alleles
Amino Acid Substitution
Budd-Chiari Syndrome complications
Budd-Chiari Syndrome diagnosis
Gene Frequency
Genotype
Humans
Myeloproliferative Disorders complications
Myeloproliferative Disorders genetics
Exome Sequencing
Budd-Chiari Syndrome genetics
Endothelial Cells metabolism
Granulocytes metabolism
Janus Kinase 2 genetics
Mutation

Full Text Access

Tools