Autor/in Kinner, M 1 Mayatepek, E 1 Meissner, T Passarge, M 1 Santer, René 1 Schaub, J 1 Schneppenheim, R Superti-Furga, A 1 alle zeigenListe einklappen
Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndrome. Santer, René Kinner, M Passarge, M Superti-Furga, A Mayatepek, E Meissner, T Schneppenheim, R 2001 - Forschungsinformationssystem des UKE
