Pathogenic variant in the X‐linked <i>ARR3</i> gene associated with variable early‐onset myopia-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Pathogenic variant in the X‐linked ARR3 gene associated with variable early‐onset myopia

Published:2023-10-05 Issue:2 Volume:194 Page:397-399
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Ediae Grace Uwaila¹²^ORCID,Chisholm Caitlin¹,Lemire Gabrielle¹²^ORCID,Campbell Fred³,Boycott Kym M.¹²^ORCID

Affiliation:

1. Regional Genetics Program, Children's Hospital of Eastern Ontario Ottawa Ontario Canada

2. Children's Hospital of Eastern Ontario Research Institute, University of Ottawa Ottawa Ontario Canada

3. Conroy Optometric Centre Ottawa Ontario Canada

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.63435

Reference11 articles.

1. Care4Rare Canada: Outcomes from a decade of network science for rare disease gene discovery

2. Control of Skeletal Patterning by EphrinB1-EphB Interactions

3. X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

4. A systematic review and meta-analysis of 271 PCDH19-variant individuals identifies psychiatric comorbidities, and association of seizure onset and disease severity

5. Mutation screening of 17 candidate genes in a cohort of 67 probands with early‐onset high myopia

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