Phenotypic overlap between pyruvate dehydrogenase complex deficiency and FOXG1 syndrome-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Phenotypic overlap between pyruvate dehydrogenase complex deficiency and FOXG1 syndrome

Published:2021-02-06 Issue:3 Volume:9 Page:1711-1715
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Akaba Yuichi¹^ORCID,Takahashi Satoru¹,Takeguchi Ryo¹,Tanaka Ryosuke¹,Nabatame Shin²,Saitsu Hirotomo³,Matsumoto Naomichi⁴

Affiliation:

1. Department of Pediatrics Asahikawa Medical University Asahikawa Japan

2. Department of Pediatrics Graduate School of Medicine Osaka University Osaka Japan

3. Department of Biochemistry Hamamatsu University School of Medicine Hamamatsu Japan

4. Department of Human Genetics Graduate School of Medicine Yokohama City University Yokohama Japan

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.3883

Reference18 articles.

1. ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology

2. FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome

4. Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant

5. Early-onset movement disorder as diagnostic marker in genetic syndromes: Three cases of FOXG1 -related syndrome

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