Overlapping neurological and cognitive phenotypes in patients with TSC1 or TSC2 mutations.
Jansen, F.E., Braams, O.B., Vincken, K.L., Algra, A., Anbeek, P., Jennekens-Schinkel, A., Halley, D., Zonnenberg, B.A., van den Ouweland, A.M.W., van Huffelen, A.C., van Nieuwenhuizen, O., Nellist, M
Neurology 70 p. 908-915