Exome sequencing reveals pathogenic mutations in the LARS2 and HSD17B4 genes associated with Perrault syndrome and D-bifunctional protein deficiency in Moroccan families
Author:
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s11033-024-09740-x.pdf
Reference45 articles.
1. Orphanet Syndrome de Perrault. https://www.orpha.net/fr/disease/detail/2855. Accessed 9 Jun 2024
2. Lerat J, Jonard L, Loundon N et al (2016) An application of NGS for Molecular investigations in Perrault Syndrome: study of 14 families and review of the literature. Hum Mutat 37:1354–1362. https://doi.org/10.1002/humu.23120
3. Soldà G, Caccia S, Robusto M et al (2016) First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family. J Hum Genet 61:295–300. https://doi.org/10.1038/jhg.2015.149
4. Roberts LM, Carnivale B (2019) Perrault Syndrome diagnosis in a patient presenting to her primary care provider with secondary Amenorrhea. Case Rep Obstet Gynecol 2019:9865281. https://doi.org/10.1155/2019/9865281
5. Jacob JJ, Paul TV, Mathews SS, Thomas N (2007) Perrault Syndrome with Marfanoid Habitus in two siblings. J Pediatr Adolesc Gynecol 20:305–308. https://doi.org/10.1016/j.jpag.2006.11.007
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