首页 | 本学科首页   官方微博 | 高级检索  
   检索      


SUCLG1 mutations and mitochondrial encephalomyopathy: a case study and review of the literature
Authors:Molaei Ramsheh  Samira  Erfanian Omidvar  Maryam  Tabasinezhad  Maryam  Alipoor  Behnam  Salmani  Tayyeb Ali  Ghaedi  Hamid
Institution:1.Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
;2.Department of Medical Laboratory Technology, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran
;3.RayeGen Daru Co, Tehran, Iran
;4.Department of Laboratory Sciences, Faculty of Paramedicine, Yasuj University of Medical Sciences, Yasuj, Iran
;
Abstract:Molecular Biology Reports - The mitochondrial encephalomyopathies represent a clinically heterogeneous group of neurodegenerative disorders. The clinical phenotype of patients could be explained by...
Keywords:
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号