医学文献 >>
  • 检索发现
  • 增强检索
知识库 >>
  • 临床诊疗知识库
  • 中医药知识库
评价分析 >>
  • 机构
  • 作者
默认
×
热搜词:
换一批
论文 期刊
取消
高级检索

检索历史 清除

Functional signatures of de novo GABBR1 and GABBR2 variants associated with neurodevelopmental disorders.

广告
第一作者: Michal,Stawarski
第一单位: Department of Biomedicine, University of Basel, Basel, Switzerland.
作者单位: Department of Biomedicine, University of Basel, Basel, Switzerland. [1] QR Genetics, Tel Aviv, Israel. [2] Valley Children's Clinic, Renton, WA, USA. [3] MultiCare Center for Weight Loss & Wellness, Covington, WA, USA. [4] Department of Clinical Genetics, Maastricht UMC+, Maastricht, the Netherlands. [5] Center of Genomic Medicine, University of Medicine and Pharmacy "Victor Babes", Timisoara, Romania.;Regional Center of Medical Genetics Timis, Clinical Emergency Hospital for Children "Louis Turcanu" part of ERN ITHACA, Timisoara, Romania. [6] Department of Clinical Genetics, Nottingham University Hospitals NHS Trust, Nottingham, England. [7] East Midlands Regional Genetics Service, Nottingham University Hospitals NHS Trust, Nottingham, England. [8] Department of Medical Genetics, Warsaw Medical University, Warsaw, Poland. [9] Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland. [10] Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.;Department of Genetic Medicine and Development, University of Geneva, Geneva, Switzerland. [11] Department of Biomedicine, University of Basel, Basel, Switzerland. bernhard.bettler@unibas.ch. [12]
DOI 10.1038/s41525-026-00558-z
PMID 41803176
发布时间 2026-04-25
提交
  • 浏览1
NPJ genomic medicine

NPJ genomic medicine

2026年11卷1期

相似文献

  • 中文期刊
  • 外文期刊
  • 学位论文
  • 会议论文

加载中!

加载中!

加载中!

加载中!

法律状态公告日 法律状态 法律状态信息

特别提示:本网站仅提供医学学术资源服务,不销售任何药品和器械,有关药品和器械的销售信息,请查阅其他网站。

  • 客服热线:4000-115-888 转3 (周一至周五:8:00至17:00)

  • |
  • 客服邮箱:yiyao@wanfangdata.com.cn

  • 违法和不良信息举报电话:4000-115-888,举报邮箱:problem@wanfangdata.com.cn,举报专区

官方微信
万方医学小程序
new医文AI 翻译 充值 订阅 收藏 移动端

官方微信

万方医学小程序

使用
帮助
Alternate Text
调查问卷