2 Einträge gefunden

1. Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndrome.

   1. Santer, René
   2. Kinner, M
   3. Passarge, M
   4. Superti-Furga, A
   5. Mayatepek, E
   6. Meissner, T
   7. Schneppenheim, R

   2001 - Forschungsinformationssystem des UKE
2. Molecular genetic basis and prevalence of glycogen storage disease type IIIA in the Faroe Islands.

   1. Santer, René
   2. Kinner, M
   3. Steuerwald, U
   4. Kjaergaard, S
   5. Skovby, F
   6. Simonsen, H
   7. Shaiu, W L

   2001 - Forschungsinformationssystem des UKE