 | Up a level |
2017
Wolking, S., Stapleton, C., Schulz, H., Nies, A., McCormack, M., Schubert, J., Schwab, M., Sander, T., Cavalleri, G. and Lerche, H. (2017). THE IDENTIFICATION FOR PHARMACOGENETIC BIOMARKERS IN THE TREATMENT OF EPILEPSY. Epilepsia, 58. S. S119 - 1. HOBOKEN: WILEY. ISSN 1528-1167
2014
Assereto, S., Robbiano, A., Di Rocco, M., Rossi, A., Cassandrini, D., Panicucci, C., Brigati, G., Biancheri, R., Bruno, C., Minetti, C., Trucks, H., Sander, T., Zara, F. and Gazzerro, E. (2014). Functional characterization of the c.462delA mutation in the NDUFS4 subunit gene of mitochondrial complex I. Clin. Genet., 86 (1). S. 99 - 102. HOBOKEN: WILEY-BLACKWELL. ISSN 1399-0004