Anders Molven
Center for Medical Genetics and Molecular Medicine
Haukeland University Hospital
Bergen
Norway
Name/email consistency: high
- A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation. Molven, A., Grimstvedt, M.B., Steine, S.J., Harland, M., Avril, M.F., Hayward, N.K., Akslen, L.A. Genes. Chromosomes. Cancer (2005)
- Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation. Molven, A., Matre, G.E., Duran, M., Wanders, R.J., Rishaug, U., Njølstad, P.R., Jellum, E., Søvik, O. Diabetes (2004)
- Hunting for a hypoglycemia gene: severe neonatal hypoglycemia in a consanguineous family. Molven, A., Rishaug, U., Matre, G.E., Njølstad, P.R., Søvik, O. Am. J. Med. Genet. (2002)