Fingerprint
Dive into the research topics of 'A homozygous loss-of-function camk2a mutation causes growth delay, frequent seizures and severe intellectual disability'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
A homozygous loss-of-function camk2a mutation causes growth delay, frequent seizures and severe intellectual disability
Poh Hui Chia*, Franklin Lei Zhong, Shinsuke Niwa, Carine Bonnard, Kagistia Hana Utami, Ruizhu Zeng, Hane Lee, Ascia Eskin, Stanley F. Nelson, William H. Xie, Samah Al-Tawalbeh, Mohammad El-Khateeb, Mohammad Shboul, Mahmoud A. Pouladi, Mohammed Al-Raqad, Bruno Reversade
*Corresponding author for this work
Research output: Contribution to journal › Article › peer-review
52
Citations
(Scopus)