A Rare Big Chinese Family With Thrombocytopenia 2: A Case Report and Literature Review-Reference-Cited by-同舟云学术

A Rare Big Chinese Family With Thrombocytopenia 2: A Case Report and Literature Review

Published:2020-04-15 Issue: Volume:11 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Tan Chengning,Dai Limeng,Chen Zhengqiong,Yang Wuchen,Wang Yali,Zeng Cheng,Xiang Zheng,Wang Xiaojie,Zhang Xiaomei,Ran Qian,Guo Hong,Li Zhongjun,Chen Li

Publisher

Frontiers Media SA

Subject

Genetics (clinical),Genetics,Molecular Medicine

Reference30 articles.

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2. A novel ANKRD26 gene variant causing inherited thrombocytopenia in a family of Finnish origin: another brick in the wall?;Averina;Thromb. Res.,2017

3. Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation.;Bluteau;J. Clin. Invest.,2014

4. Childhood diagnosis of genetic thrombocytopenia with mutation in the ankyrine repeat domain 26 gene.;Boutroux;Eur. J. Pediatr.,2015

5. A novel nucleotide substitution in the 5′ untranslated region of ANKRD26 gene is associated with inherited thrombocytopenia: a report of two new families.;Diep;Ann. Hematol.,2019

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3. Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases;Platelets;2022-05-19

4. Potential biomarkers for inherited thrombocytopenia 2 identified by plasma proteomics;Platelets;2021-06-08

5. Familial thrombocytopenia due to a complex structural variant resulting in a WAC-ANKRD26 fusion transcript;Journal of Experimental Medicine;2021-04-15