Prader-Willi Syndrome and Schaaf-Yang Syndrome: Neurodevelopmental Diseases Intersecting at the MAGEL2 Gene
Author:
Publisher
MDPI AG
Link
http://www.mdpi.com/2079-9721/4/1/2/pdf
Reference23 articles.
1. Prader-Willi syndrome
2. Prader-Willi syndrome: Consensus diagnostic criteria;Holm;Pediatrics,1993
3. Prader–Willi syndrome and autism spectrum disorders: an evolving story
4. Cognitive and behavioural aspects of Prader–Willi syndrome
5. Behavior in Prader-Willi syndrome: relationship to genetic subtypes and age
Cited by 72 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. Truncated variants of MAGEL2 are involved in the etiologies of the Schaaf-Yang and Prader-Willi syndromes;The American Journal of Human Genetics;2024-07
2. MAGEL2 (patho‐)physiology and Schaaf–Yang syndrome;Developmental Medicine & Child Neurology;2024-07
3. Acquiring Social Safety Engages Oxytocin Neurons in the Supraoptic Nucleus: Role of Magel2 Deficiency;Neuroendocrinology;2024-04-04
4. Subcellular localisation of truncated MAGEL2 proteins: insight into the molecular pathology of Schaaf-Yang syndrome;Journal of Medical Genetics;2024-03-28
5. Special clinical manifestations and genetic characteristics of schaaf–Yang syndrome in Russian patients;Neuromuscular Diseases;2024-03-01
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