Work

A novel splice donor mutation in the thrombopoietin gene leads to exon 2 skipping in a Filipino family with hereditary thrombocythemia

Year: 2011

Type: article

Abstract: To the editor: In contrast to the familial predisposition observed in somatically acquired myeloproliferative neoplasms (low penetrance, clonal hematopoiesis), the hereditary thrombocythemias (HT) are characterized by Mendelian inheritance, high penetrance, and polyclonal hematopoiesis, and appear

Source: Blood

DOI: 10.1182/blood-2011-10-386177

Authors: Bing Zhang, Dana Ng, Carol Jones, Stephen T. Oh, Garry P. Nolan, Shiva Salehi, Wendy Wong, James L. Zehnder, Jason Gotlib

Institutions: Stanford Medicine, Stanford University, Washington University in St. Louis, Stanford Cancer Institute

Language: English

Topic: Platelet Disorders and Treatments

Subfield: Hematology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: National Institutes of Health, National Cancer Institute

Awards: Modeling the Role of Differentiation in Cancer Progression, G2704802626, Multi-scale Complex Systems Transdisciplinary Analysis of Response to Therapy (MC, Software & Hardware Inference Engines for Automated Determination of Primary Cell

OpenAlex ID: W2035451212

FWCI: 1.045

Cites: 6

Cited by: 15

Related to: 10