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Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: Evidence for different origins of common mutations

M. Witsch-Baumgartner, E. Ciara, J. Löffler, H. J. Menzel, U. Seedorf, J. Burn, G. Gillessen-Kaesbach, G. F. Hoffmann, B. U. Fitzky, H. Mundy, P. Clayton, R. I. Kelley, M. Krajewska-Walasek, G. Utermann*

*Corresponding author for this work
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