De Novo Mutations of CCNK Cause a Syndromic Neurodevelopmental Disorder with Distinctive Facial Dysmorphism-Reference-Cited by-同舟云学术

De Novo Mutations of CCNK Cause a Syndromic Neurodevelopmental Disorder with Distinctive Facial Dysmorphism

Published:2018-09 Issue:3 Volume:103 Page:448-455
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Fan Yanjie,Yin Wu,Hu Bing,Kline Antonie D.,Zhang Victor Wei,Liang Desheng,Sun Yu,Wang Lili,Tang Sha,Powis Zöe,Li Lei,Yan Huifang,Shi Zhen,Yang Xiaoping,Chen Yinyin,Wang Jingmin,Jiang Yuwu,Tan Hu,Gu Xuefan,Wu Lingqian,Yu Yongguo^ORCID

Funder

National Natural Science Foundation of China

Shanghai Municipal Education Commission

Jiaotong University Cross Biomedical Engineering

Shanghai Municipal Commission of Health and Family Planning

Shanghai Shen Kang Hospital Development Center new frontier technology joint project

China Postdoctoral Science Foundation

Fundamental Research Funds for the Central Universities

National Key R&D Program of China

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference17 articles.

1. Principles of Neural Science;Kandel,2013

2. Prevalence of intellectual disability: a meta-analysis of population-based studies;Maulik;Res. Dev. Disabil.,2011

3. Comprehensive evaluation of the child with intellectual disability or global developmental delays;Moeschler;Pediatrics,2014

4. Genome sequencing identifies major causes of severe intellectual disability;Gilissen;Nature,2014

5. Cdks, cyclins and CKIs: roles beyond cell cycle regulation;Lim;Development,2013

Cited by 16 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. Macrocephaly and Finger Changes: A Narrative Review;International Journal of Molecular Sciences;2024-05-20

2. Intellectual developmental disorder with hypertelorism and distinctive facies (IDDHDF) A case study with literature review;Journal of Health Science and Medical Therapy;2024-03-06

3. CCNK Gene Deficiency Influences Neural Progenitor Cells Via Wnt5a Signaling in CCNK‐Related Syndrome;Annals of Neurology;2023-09-13

4. Modelling Autism Spectrum Disorder (ASD) and Attention-Deficit/Hyperactivity Disorder (ADHD) Using Mice and Zebrafish;International Journal of Molecular Sciences;2022-07-07