谷歌浏览器插件
订阅小程序
在清言上使用
VIPCreated with Sketch.

An FBN1 Deep Intronic Mutation in a Familial Case of Marfan Syndrome: an Explanation for Genetically Unsolved Cases?

Elisabeth Gillis,Marlies Kempers,Simone Salemink,Janneke Timmermans,Emile C. Cheriex,Sebastiaan C. A. M. Bekkers,Erik Fransen,Christine E. M. De Die-Smulders,Bart L. Loeys,Lut Van Laer

Human Mutation（2014）

引用 34|浏览25
暂无评分
关键词
Marfan syndrome,deep intronic mutation,FBN1,pseudo-exon
AI 理解论文
溯源树
样例
生成溯源树，研究论文发展脉络
Chat Paper
正在生成论文摘要