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


Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency
Institution:1. Wellcome Trust Centre for Mitochondrial Research, Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne NE2 4HH, UK;2. Child Development Centre, Addenbrooke''s Hospital, Cambridge, UK;3. Medical Genetics Laboratories, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK;4. Department of Medical Genetics, Addenbrookes Hospital, Cambridge, UK;5. Biobank, Institute for Genetic Medicine, Newcastle University, International Centre for Life, Central Parkway, Newcastle upon Tyne NE1 3BZ, UK;6. The Wellcome Trust Centre for Mitochondrial Research, Institute for Cell and Molecular Biosciences, Newcastle University, Newcastle upon Tyne NE2 4HH, UK
Abstract:
Keywords:
本文献已被 ScienceDirect 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