Chia PH, Zhong FL, Niwa S, Bonnard C, Utami KH, Zeng R, Lee H, Eskin A, Nelson SF, Xie WH, Al-Tawalbeh S, El-Khateeb M, Shboul M, Pouladi MA, Al-Raqad M, Reversade B.
Elife, 2018
Summary:
Explore how Maestro MEA technology helped to reveal how a recessive germline mutation in CAMK2A leads to neurodevelopmental defects and may contribute to other neurological disorders.
