Clinical and molecular heterogeneity of VPS13D-related neurodevelopmental and movement disorders-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Clinical and molecular heterogeneity of VPS13D-related neurodevelopmental and movement disorders

Published:2024-03 Issue: Volume:899 Page:148119
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Sultan Tipu,Scorrano Giovanna,Panciroli Marta,Christoforou Marilena,Raza Alvi Javeria,Di Ludovico Armando,Qureshi Sameen,Efthymiou Stephanie^ORCID,Salpietro Vincenzo,Houlden Henry

Funder

Wellcome Trust

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference49 articles.

1. Vps13D Encodes a ubiquitin-binding protein that is required for the regulation of mitochondrial size and clearance;Anding;Curr. Biol.,2018

2. Brain organoids as model systems for genetic neurodevelopmental disorders;Baldassari;Front. Cell Dev. Biol.,2020

3. VPS13D promotes peroxisome biogenesis;Baldwin;J. Cell Biol.,2021

4. Competitive organelle-specific adaptors recruit Vps13 to membrane contact sites;Bean;J. Cell Biol.,2018

5. The neuroimaging of Leigh syndrome: case series and review of the literature;Bonfante;Pediatr. Radiol.,2016

Cited by 2 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. Clinical, genetic, and neuroimaging profiles of autosomal recessive spinocerebellar ataxia type 4 caused by novel VPS13D variants in Chinese;American Journal of Medical Genetics Part A;2024-07-26

2. Comparison of Growth Performance, Nutritional Composition, and Muscle Transcriptome between Two Cultured Varieties of the Chinese Mitten Crab (Eriocheir sinensis);Fishes;2024-04-09

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