A novel ANKRD26 gene variant causing inherited thrombocytopenia in a family of Finnish origin: Another brick in the wall?
Author:
Publisher
Elsevier BV
Subject
Hematology
Reference8 articles.
1. Inherited thrombocytopenias frequently diagnosed in adults;Baldini;J. Thromb. Haemost.,2013
2. 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
3. Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families;Norris;Blood,2011
4. To the editor: a missense mutation in ANKRD26 segregates with thrombocytopenia;Al Daama;Blood,2013
5. Inherited thrombocytopenias. The evolving spectrum;Balduini;Hamostaseologie,2012
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1. Analysis of clinical characteristics and treatment efficacy in two pediatric cases of ANKRD26 -related thrombocytopenia;Platelets;2023-10-18
2. Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases;Platelets;2022-05-19
3. Potential biomarkers for inherited thrombocytopenia 2 identified by plasma proteomics;Platelets;2021-06-08
4. A Rare Big Chinese Family With Thrombocytopenia 2: A Case Report and Literature Review;Frontiers in Genetics;2020-04-15
5. Observation of granulocyte function during ex vivo thrombus formation for patients with ANKRD26-associated thrombocytopenia;Pediatric Hematology/Oncology and Immunopathology;2020-03-28
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