<b><i>GATAD2B</i></b> Gene Microdeletion Causing Intellectual Disability Autosomal Dominant Type 18: Case Report and Review of the Literature-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

GATAD2B Gene Microdeletion Causing Intellectual Disability Autosomal Dominant Type 18: Case Report and Review of the Literature

Published:2019 Issue:4 Volume:10 Page:186-194
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Trubnykova Milana,Bazalar Montoya Jeny,La Serna-Infantes Jorge,Vásquez Sotomayor Flor,Castro Mujica María del Carmen,Abarca Barriga Hugo Hernán

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Reference23 articles.

1. Allen HF, Wade PA, Kutateladze TG: The NuRD architecture. Cell Mol Life Sci 70:3513-3524 (2013).

2. Brackertz M, Boeke J, Zhang R, Renkawitz R: Two highly related p66 proteins comprise a new family of potent transcriptional repressors interacting with MBD2 and MBD3. J Biol Chem 277:40958-40966 (2002).

3. Chiurazzi P, Pirozzi F: Advances in understanding - genetic basis of intellectual disability. F1000Res 5:F1000 Faculty Rev-599 (2016).

4. de Ligt J, Willemsen MH, van Bon BW, Kleefstra T, Yntema HG, et al: Diagnostic exome sequencing in persons with severe intellectual disability. N Engl J Med 367:1921-1929 (2012).

5. Feng Q, Zhang Y: MeCP1 complex represses transcription through preferential binding, remodeling, and deacetylating methylated nucleosomes. Genes Dev 15:827-832 (2001).

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Defining the Dynamic Regulation of O-GlcNAc Proteome in the Mouse Cortex---the O-GlcNAcylation of Synaptic and Trafficking Proteins Related to Neurodegenerative Diseases;Frontiers in Aging;2021-09-29

2. A genome-wide association study identifies a gene network associated with paranoid schizophrenia and antipsychotics-induced tardive dyskinesia;Progress in Neuro-Psychopharmacology and Biological Psychiatry;2021-03

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3