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Number of items: 4.

Göhring, I; Tagariello, A; Endele, S; Stolt, C C; Ghassibé, M; Fisher, M; Thiel, C T; Trautmann, U; Vikkula, M; Winterpacht, A; FitzPatrick, D R; Rauch, A (2010). Disruption of ST5 is associated with mental-retardation and multiple congenital anomalies. Journal of Medical Genetics, 47(2):91-98.

Wiame, E; Tyteca, D; Pierrot, N; Collard, F; Amyere, M; Noel, G; Desmedt, J; Nassogne, M C; Vikkula, M; Octave, J N; Vincent, M F; Courtoy, P J; Boltshauser, E; van Schaftingen, E (2010). Molecular identification of aspartate N-acetyltransferase and its mutation in hypoacetylaspartia. Biochemical Journal, 425(1):127-136.

Coutelier, M; Andries, S; Ghariani, S; Dan, B; Duyckaerts, C; van Rijckevorsel, K; Raftopoulos, C; Deconinck, N; Sonderegger, P; Scaravilli, F; Vikkula, M; Godfraind, C (2008). Neuroserpin mutation causes electrical status epilepticus of slow-wave sleep. Neurology, 71(1):64-66.

Revencu, N; Boon, L M; Mulliken, J B; Enjolras, O; Cordisco, M R; Burrows, P E; Clapuyt, P; Hammer, F; Dubois, J; Baselga, E; Brancati, F; Carder, R; Quintal, J M C; Dallapiccola, B; Fischer, G; Frieden, I J; Garzon, M; Harper, J; Johnson-Patel, J; Labrèze, C; Martorell, L; Paltiel, H J; Pohl, A; Prendiville, J; Quere, I; Siegel, D H; Valente, E M; Van Hagen, A; Van Hest, L; Vaux, K K; Vicente, A; Weibel, L; Chitayat, D; Vikkula, M (2008). Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused by RASA1 mutations. Human Mutation, 29(7):959-965.

This list was generated on Tue Jul 25 04:12:44 2017 CEST.