Busk, Øyvind Løvold

De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability

Küry, S., van Woerden, G. M., Besnard, T., Proietti Onori, M., Latypova, X., Towne, M. C., Cho, M. T., Prescott, T. E., Ploeg, M. A., Sanders, S., et al. (2017) · The American Journal of Human Genetics

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 185

Identification of surface proteins in Enterococcus faecalis V583

Bøhle, L. A., Riaz, T., Egge-Jacobsen, W., Skaugen, M., Busk, Ø. L., Eijsink, V. G., & Mathiesen, G. (2011) · BMC Genomics

Advanced Proteomics Techniques and ApplicationsBacterial Genetics and Biotechnology

Cited by 67

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

Stamberger, H., Hammer, T. B., Gardella, E., Vlaskamp, D. R. M., Bertelsen, B., Mandelstam, S., de Lange, I., Zhang, J., Myers, C. T., Fenger, C., et al. (2021) · Genetics in Medicine

Genetics and Neurodevelopmental DisordersEpilepsy research and treatment

Cited by 57