Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome

Sandra Ammann, Ansgar Schulz, Ingeborg Krägeloh-Mann, Nele M G Dieckmann, Klaus Niethammer, Sebastian Fuchs, Katja Martina Eckl, Roswitha Plank, Roland Werner, Janine Altmüller, Holger Thiele, Peter Nürnberg, Julia Bank, Anne Strauss, Horst Von Bernuth, Udo Zur Stadt, Samantha Grieve, Gillian M. Griffiths, Kai Lehmberg, Hans Christian HenniesStephan Ehl

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Hans Hennies
- H.C.Hennies@hud.ac.uk
- Department of Biological and Geographical Sciences - Reader in Molecular Biology
- School of Applied Sciences
- Cellular and Molecular Models of Disease Centre - Director
- Centre for Biomarker Research - Associate Member
- Evolutionary Genomics Research Centre - Secondary Membership
- Pharmaceutics and Drug Delivery Centre - Associate Member
Person: Academic

Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome

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Hans Hennies