3 Einträge gefunden

1. An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome

   1. Abdollahpour, Hengameh
   2. Alawi, Malik
   3. Kortüm, Fanny
   4. Beckstette, Michael
   5. Seemanova, Eva
   6. Komárek, Vladimír
   7. Rosenberger, Georg

   2015 - Forschungsinformationssystem des UKE
2. αPIX Is a Trafficking Regulator that Balances Recycling and Degradation of the Epidermal Growth Factor Receptor

   1. Kortüm, Fanny
   2. Harms, Frederike Leonie
   3. Hennighausen, Natascha
   4. Rosenberger, Georg

   2015 - Forschungsinformationssystem des UKE - frei zugänglich
3. Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome

   1. Kortüm, Fanny
   2. Caputo, Viviana
   3. Bauer, Christiane K
   4. Stella, Lorenzo
   5. Ciolfi, Andrea
   6. Alawi, Malik
   7. Bocchinfuso, Gianfranco

   2015 - Forschungsinformationssystem des UKE