De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females

R. Webster, M. T. Cho, K. Retterer, F. Millan, C. Nowak, J. Douglas, A. Ahmad, G. V. Raymond, M. R. Johnson, A. Pujol, A. Begtrup, D. McKnight, O. Devinsky, W. K. Chung

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Fingerprint

Dive into the research topics of 'De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females'. Together they form a unique fingerprint.

Medicine & Life Sciences