Preserved speech variants of the Rett syndrome: Molecular and clinical analysis
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference27 articles.
1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
2. Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes
3. MECP2 mutations account for most cases of typical forms of Rett syndrome
4. Diagnostic Testing for Rett Syndrome by DHPLC and Direct Sequencing Analysis of the MECP2 Gene: Identification of Several Novel Mutations and Polymorphisms
5. The Methyl-CpG Binding Transcriptional Repressor MeCP2 Stably Associates with Nucleosomal DNA
Cited by 109 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. Distributed X chromosome inactivation in brain circuitry is associated with X-linked disease penetrance of behavior;Cell Reports;2024-04
2. POMC-specific knockdown of MeCP2 leads to adverse phenotypes in mice chronically exposed to high fat diet;Behavioural Brain Research;2024-03
3. Atypical brain responses to 40‐Hz click trains in girls with Rett syndrome: Auditory steady‐state response and sustained wave;Psychiatry and Clinical Neurosciences;2024-02-06
4. Use of Augmentative and Alternative Communication by Individuals with Rett Syndrome Part 2: High-Tech and Low-Tech Modalities;Journal of Developmental and Physical Disabilities;2023-04-14
5. Pomc-Specific Knockdown of Mecp2 Leads to Adverse Phenotypes in Mice Chronically Exposed to High Fat Diet;2023
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