A novel nucleotide substitution in the 5 untranslated region of ANKRD26 gene is associated with inherited thrombocytopenia: a report of two new families

Diep Robert T.; Corey Kristin; Arcasoy Murat O.

首页> 外文期刊>Annals of hematology >A novel nucleotide substitution in the 5 untranslated region of ANKRD26 gene is associated with inherited thrombocytopenia: a report of two new families

【24h】

A novel nucleotide substitution in the 5 untranslated region of ANKRD26 gene is associated with inherited thrombocytopenia: a report of two new families

机译：ANKRD26基因的5个未翻译区域中的新核苷酸取代与遗传血小板减少症有关：两个新家庭的报告

获取原文

获取原文并翻译 | 示例

获取外文期刊封面封底 >>

开具论文收录证明 >>

文献代查 >>

页面导航

著录项
相似文献
相关主题

著录项

来源
《Annals of hematology》 |2019年第7期|共3页
作者
Diep Robert T.; Corey Kristin; Arcasoy Murat O.;
展开▼
作者单位

Duke Univ Sch Med Dept Med Div Hematol Durham NC 27710 USA;

Duke Univ Sch Med Dept Med Div Hematol Durham NC 27710 USA;

Duke Univ Sch Med Dept Med Div Hematol Durham NC 27710 USA;

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类血液及淋巴系疾病;
关键词

相似文献

外文文献
中文文献
专利

1. A novel nucleotide substitution in the 5 untranslated region of ANKRD26 gene is associated with inherited thrombocytopenia: a report of two new families [J] . Diep Robert T., Corey Kristin, Arcasoy Murat O. Annals of hematology . 2019,第7期

机译：ANKRD26基因的5个未翻译区域中的新核苷酸取代与遗传血小板减少症有关：两个新家庭的报告
2. A novel ANKRD26 gene variant causing inherited thrombocytopenia in a family of Finnish origin: Another brick in the wall? [J] . Averina M., Jensvoll H., Strand H., Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis . 2017,第期

机译：一种新的ANKRD26基因变体，导致芬兰血统遗传血小板减少症：墙上的另一块砖？
3. Strong association of a single nucleotide substitution in the 3'-untranslated region of the apolipoprotein-CIII gene with common hypertriglyceridemia in Arabs. [J] . S Ta? Clinical Chemistry: Journal of the American Association for Clinical Chemists . 1989,第2期

机译：载脂蛋白-CIII基因3'-非翻译区的单核苷酸取代与阿拉伯人常见的高甘油三酯血症有很强的联系。
4. NUCLEOTIDE SUBSTITUTIONS AND THE EVOLUTION OF DUPLICATE GENES [C] . JOHN S. CONERY, MICHAEL LYNCH Pacific Symposium on Biocomputing 2001, Jan 3-7, 2001, Mauna Lani, Hawaii . 2001

机译：核苷酸取代和双倍基因的进化
5. Patterns of nucleotide substitution within and among mitochondrial gene regions in sea stars (Leptasterias spp.) [D] . Hrincevich, Adam Wayne 2002

机译：海星（Leptasterias spp。）线粒体基因区域内和之间的核苷酸取代模式
6. An Autosomal Dominant Cerebellar Ataxia Linked to Chromosome 16q22.1 Is Associated with a Single-Nucleotide Substitution in the 5′ Untranslated Region of the Gene Encoding a Protein with Spectrin Repeat and Rho Guanine-Nucleotide Exchange-Factor Domains [O] . Kinya Ishikawa, Shuta Toru, Taiji Tsunemi, 2005

机译：与染色体16q22.1连锁的常染色体显性小脑共济失调与编码具有血影蛋白重复和Rho鸟嘌呤-核苷酸交换因子结构域的蛋白质的基因的5非翻译区中的单核苷酸取代相关。
7. An Autosomal Dominant Cerebellar Ataxia Linked to Chromosome 16q22.1 Is Associated with a Single-Nucleotide Substitution in the 5′ Untranslated Region of the Gene Encoding a Protein with Spectrin Repeat and Rho Guanine-Nucleotide Exchange-Factor Domains [O] . Ishikawa Kinya, Toru Shuta, Tsunemi Taiji, 2005

机译：与染色体16q22.1连锁的常染色体显性小脑共济失调与编码具有血影蛋白重复和Rho鸟嘌呤-核苷酸交换因子结构域的蛋白质的基因的5'非翻译区中的单核苷酸取代相关。

A novel nucleotide substitution in the 5 untranslated region of ANKRD26 gene is associated with inherited thrombocytopenia: a report of two new families

著录项

相似文献

相关主题

期刊订阅