GATA1 gene variants associated with thrombocytopenia and anemia

Freson Kathleen; Wijgaerts Anouck; Van Geet Chris

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GATA1 gene variants associated with thrombocytopenia and anemia

机译：GATA1与血小板减少症和贫血相关的基因变体

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来源
《Platelets》 |2017年第7期|共4页
作者
Freson Kathleen; Wijgaerts Anouck; Van Geet Chris;
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作者单位

Katholieke Univ Leuven Ctr Mol &

Vasc Biol Dept Cardiovasc Sci Leuven Belgium;

Katholieke Univ Leuven Ctr Mol &

Vasc Biol Dept Cardiovasc Sci Leuven Belgium;

Katholieke Univ Leuven Ctr Mol &

Vasc Biol Dept Cardiovasc Sci Leuven Belgium;

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原文格式 PDF
正文语种 eng
中图分类基础医学;
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1. GATA1 gene variants associated with thrombocytopenia and anemia [J] . Freson Kathleen, Wijgaerts Anouck, Van Geet Chris Platelets . 2017,第7期

机译：GATA1与血小板减少症和贫血相关的基因变体
2. FUNCTIONAL ANALYSIS OF HETEROZYGOUS GATA1 DELETERIOUS MUTATIONS IN TWO CHINESE FEMALE PATIENTS AFFECTED BY DYSERYTHROPOIETIC ANEMIA, THROMBOCYTOPENIA AND PORPHYRIA, RESPECTIVELY [J] . Wang Yongwei, Liu Gang, Guo Shanshan, American Journal of Hematology . 2017,第8期

机译：两种中国女性患者杂合性贫血患者的杂合性GATA 1有害突变的功能分析
3. A PATIENT WITH MACROCYTIC ANEMIA AND PLATELET DYSFUNCTION ASSOCIATED WITH A NOVEL VARIANT OF GATA1 MUTATION [J] . Li Yixian, Manalang Michelle, McManus Michael Pediatric blood & cancer . 2018,第Suppla1期

机译：患有大核贫血和血小板功能障碍的患者与GATA1突变的新变种相关
4. DIAGNOSIS OF IMMUNE-MEDIATED HEMOLYTIC ANEMIA AND THROMBOCYTOPENIA [C] . Andrew Mackin Annual Meeting of the American Animal Hospital Association . 2004

机译：免疫介导的溶血性贫血和血小板减少症的诊断
5. Heterogeneity Within Primary Progressive Aphasia (PPA): Differences Between Variants in Functional Communication, and a New Sub-Variant of Logopenic Variant PPA [D] . Gallée, Jeanne. 2021

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6. Loss of the Gata1 Gene IE Exon Leads to Variant Transcript Expression and the Production of a GATA1 Protein Lacking the N-terminal Domain [O] . Eri Kobayashi, Ritsuko Shimizu, Yuko Kikuchi, 2010

机译：Gata1基因IE外显子的丢失导致变异的转录表达和缺乏N末端域的GATA1蛋白的生产。
7. Novel G6B gene variant causes familial autosomal recessive thrombocytopenia and anemia [O] . Motasem Melhem, Mohamed Abu-Farha, Dinu Antony, 2017

机译：新型G6B基因变体导致家族性常染色体隐性血小板减少症和贫血

GATA1 gene variants associated with thrombocytopenia and anemia

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