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Research | 28 June 2009
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II
- klaus.schwarz@uni-ulm.de
- Klaus Schwarz
- , Achille Iolascon
- , Fatima Verissimo
- , Nikolaus S Trede
- , Wyatt Horsley
- , Wen Chen
- , Barry H Paw
- , Karl-Peter Hopfner
- , Karlheinz Holzmann
- , Roberta Russo
- , Maria Rosaria Esposito
- , Daniela Spano
- , Luigia De Falco
- , Katja Heinrich
- , Brigitte Joggerst
- , Markus T Rojewski
- , Silverio Perrotta
- , Jonas Denecke
- , Ulrich Pannicke
- , Jean Delaunay
- , Rainer Pepperkok
- & Hermann Heimpel
Nature Genetics 41 , 936–940

Rights & permissionsfor article Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II . Opens in a new window.
Research | 30 November 2008
Reticular dysgenesis (aleukocytosis) is caused by mutations in the gene encoding mitochondrial adenylate kinase 2
- klaus.schwarz@uni-ulm.de
- Ulrich Pannicke
- , Manfred Hönig
- , Isabell Hess
- , Claudia Friesen
- , Karlheinz Holzmann
- , Eva-Maria Rump
- , Thomas F Barth
- , Markus T Rojewski
- , Ansgar Schulz
- , Thomas Boehm
- , Wilhelm Friedrich
- & Klaus Schwarz
Nature Genetics 41 , 101–105

Rights & permissionsfor article Reticular dysgenesis (aleukocytosis) is caused by mutations in the gene encoding mitochondrial adenylate kinase 2 . Opens in a new window.
Reviews | 1 September 2003
Mechanism and regulation of human non-homologous DNA end-joining
- klaus.schwarz@medizin.uni-ulm.de
Nature Reviews Molecular Cell Biology 4 , 712–720

Rights & permissionsfor article Mechanism and regulation of human non-homologous DNA end-joining . Opens in a new window.

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