Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis

Published:2019-04-26 Issue:1 Volume:10 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Fotiou Elisavet,Martin-Almedina Silvia,Simpson Michael A.,Lin Shin,Gordon Kristiana,Brice Glen,Atton Giles,Jeffery Iona,Rees David C.,Mignot Cyril,Vogt Julie,Homfray Tessa,Snyder Michael P.,Rockson Stanley G.,Jeffery Steve,Mortimer Peter S.,Mansour Sahar,Ostergaard Pia

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/s41467-019-09905-4.pdf

Cited by 5 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. PIEZO1 is the most common monogenic etiology of non‐immune hydrops fetalis detected by prenatal exome sequencing;Prenatal Diagnosis;2023-10-30

2. A very rare disease of lymphatic malformation 6: five new patients and review of the literatur;Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi;2023-06-30

3. Mechanosensitive Ion Channels, Axonal Growth, and Regeneration;The Neuroscientist;2022-04-13

4. A New Hope in Spinal Degenerative Diseases: Piezo1;BioMed Research International;2021-01-25

5. Molecular Biology of the Nociceptor/Transduction;The Senses: A Comprehensive Reference;2020

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