Tveten, Kristian

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

PCSK9 acts as a chaperone for the LDL receptor in the endoplasmic reticulum

Strøm, T. B., Tveten, K., & Leren, T. P. (2014) · Biochemical Journal

Cholesterol and Lipid MetabolismLipoproteins and Cardiovascular Health

Cited by 48