Cuno, Stephan M.
Helmholtz Munich · UCL Queen Square Institute of Neurology · Institut für Humangenetik · University College London · Technical University of Munich
2 papers on CoChat
Most cited papers
- Verified
Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA
Haack, T. B., Hogarth, P., Kruer, M. C., Gregory, A., Wieland, T., Schwarzmayr, T., Graf, E., Sanford, L., Meyer, E., Kara, E., et al. (2012) · The American Journal of Human Genetics
Neurological diseases and metabolismIron Metabolism and Disorders
Cited by 360
- Verified
Beta-propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation
Hayflick, S. J., Kruer, M. C., Gregory, A., Haack, T. B., Kurian, M. A., Houlden, H. H., Anderson, J., Boddaert, N., Sanford, L., Harik, S. I., et al. (2013) · Brain
Neurological diseases and metabolismIron Metabolism and Disorders
Cited by 250
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