Association of Cole disease with novel heterozygous mutations in the somatomedin‐B domains of the ENPP1 gene: necessary, but not always sufficient. (1st May 2016) - Schlipf, N.A.; Traupe, H.; Gilaberte, Y.; Peitsch, W.K.; Hausser, I.; Oji, V.; Schmieder, A.; Schneider, S.W.; Demmer, P.; Rösler, B.; Fischer, J.