Case Report
Published on 24 Jan 2022
Case Report: Mutation in AIMP2/P38, the Scaffold for the Multi-Trna Synthetase Complex, and Association With Progressive Neurodevelopmental Disorders
in Genetics of Common and Rare Diseases
![Case Report: Mutation in AIMP2/P38, the Scaffold for the Multi-Trna Synthetase Complex, and Association With Progressive Neurodevelopmental Disorders](https://www.frontiersin.org/files/myhome article library/816987/816987_Thumb_400.jpg)
- 2,174 views
- 2 citations