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Uyanik, G. and Elcioglu, N. and Penzien, J. and Gross, C. and Yilmaz, Y. and Olmez, A. and Demir, E. and Wahl, D. and Scheglmann, K. and Winner, B. and Bogdahn, U. and Topaloglu, H. and Hehr, U. and Winkler, J. (2006) Novel truncating and missense mutations of the KCC3 gene associated with Andermann syndrome. Neurology 66 (7), pp. 1044-1048.