PCDH19-related infantile epileptic encephalopathy: An unusual X-linked inheritance disorder
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference47 articles.
1. Protocadherin-19 and N-cadherin interact to control cell movements during anterior neurulation;Biswas;J Cell Biol,2010
2. No evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans;Bolduc;J Clin Invest,2008
3. Screening the human protocadherin 8 (PCDH8) gene in schizophrenia;Bray;Genes Brain Behav,2002
4. Age-associated skewing of X-inactivation ratios of blood cells in normal females: a candidate-gene analysis approach;Chagnon;Exp Hematol,2005
5. Control of skeletal patterning by ephrinB1-EphB interactions;Compagni;Dev Cell,2003
Cited by 122 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. Dravet-like syndrome with PCDH19 mutations in Taiwan ― A multicenter study;Pediatrics & Neonatology;2024-08
2. Multicenter retrospective study of patients with PCDH19‐related epilepsy: The first Hungarian cohort;Epileptic Disorders;2024-07-17
3. NGS-Based Identification of Two Novel PCDH19 Mutations in Female Patients with Early-Onset Epilepsy;International Journal of Molecular Sciences;2024-05-24
4. PCDH19-clustering epilepsy, pathophysiology and clinical significance;Epilepsy & Behavior;2024-05
5. Abnormal cell sorting and altered early neurogenesis in a human cortical organoid model of Protocadherin-19 clustering epilepsy;Frontiers in Cellular Neuroscience;2024-04-04
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