Expanding the molecular basis and phenotypic spectrum of ZDHHC9 ‐associated X‐linked intellectual disability-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Expanding the molecular basis and phenotypic spectrum of ZDHHC9 ‐associated X‐linked intellectual disability

Published:2018-04-21 Issue:5 Volume:176 Page:1238-1244
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Schirwani Schaida¹^ORCID,Wakeling Emma²,Smith Kath³,Balasubramanian Meena⁴⁵^ORCID,

Affiliation:

1. Yorkshire Regional Genetics Service, Chapel Allerton HospitalLeeds Teaching Hospitals NHS TrustLeeds United Kingdom

2. North West Thames Regional Genetics ServiceLondon North West University Hospitals NHS TrustHarrow United Kingdom

3. Sheffield Diagnostic Genetics ServiceSheffield Children's NHS Foundation TrustSheffield Yorkshire United Kingdom

4. Academic Unit of Child Health, Department of Oncology & MetabolismUniversity of Sheffield United Kingdom

5. Sheffield Clinical Genetics ServiceSheffield Children's NHS Foundation TrustSheffield United Kingdom

Funder

Health Innovation Challenge Fund

Wellcome Trust Sanger Institute

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.38683

Reference14 articles.

1. Epilepsy, cognitive deficits and neuroanatomy in males with ZDHHC 9 mutations

2. Structural brain abnormalities in a single gene disorder associated with epilepsy, language impairment and intellectual disability

3. Global and Local Connectivity Differences Converge With Gene Expression in a Neurodevelopmental Disorder of Known Genetic Origin

4. Detection of clinically relevant exonic copy-number changes by array CGH

5. Targeted Next‐Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability

Cited by 15 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. Micro-Scale Control of Oligodendrocyte Morphology and Myelination by the Intellectual Disability-Linked Protein Acyltransferase ZDHHC9;2024-08-27

2. Micro-Scale Control of Oligodendrocyte Morphology and Myelination by the Intellectual Disability-Linked Protein Acyltransferase ZDHHC9;2024-08-27

3. Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature;BMC Medical Genomics;2023-10-11

4. Micro-Scale Control of Oligodendrocyte Morphology and Myelination by the Intellectual Disability-Linked Protein Acyltransferase ZDHHC9;2023-09-21

5. The X-Linked Intellectual Disability gene,ZDHHC9, is important for oligodendrocyte maturation and myelin formation;2023-08-08

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

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