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Exome sequencing identifies a novel heterozygous TGFB3 mutation in a disorder overlapping with Marfan and Loeys-Dietz syndrome.
Kuechler, A. and Altmüller, J. and Nürnberg, P. and Kotthoff, S. and Kubisch, C. and Borck, G.
Molecular and Cellular Probes 29 (5): 330-334. October 2015

Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy.
Haug, K. and Kremerskothen, J. and Hallmann, K. and Sander, T. and Dullinger, J. and Rau, B. and Beyenburg, S. and Lentze, M.J. and Barnekow, A. and Elger, C.E. and Propping, P. and Heils, A.
Molecular and Cellular Probes 14 : 255-260. 1 August 2000