A POTEntial new gene for thrombocytopenia
Author:
Affiliation:
1. RADY CHILDREN'S HOSPITAL SAN DIEGO
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/117/24/6406/1339394/zh802411006406.pdf
Reference8 articles.
1. Inherited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle Piastrine.;Balduini;Haematologica,2003
2. Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.;Noris;Blood,2011
3. Mutations in the 5′ UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2.;Pippucci;Am J Hum Genet,2011
4. A mutation of human cytochrome c enhances the intrinsic apoptotic pathway but causes only thrombocytopenia.;Morison;Nat Genet,2008
5. POTE paralogs are induced and differentially expressed in many cancers.;Bera;Cancer Res,2006
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3. Milde Blutungsneigung bei einer 62-Jährigen mit hereditärer Thrombozytopenie;Der Internist;2013-05-17
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