by Pinto, A, Alfadhel, M, Akroyd, R, Atik Altınok, Y, Bernabei, S M, Bernstein, L, Bruni, G, Caine, G, Cameron, E, Carruthers, R, Cochrane, B, Daly, A, de Boer, F, Delaunay, S, Dianin, A, Dixon, M, Drogari, E, Dubois, S, Evans, S, Gribben, J, Gugelmo, G, Heidenborg, C, Hunjan, I, Kok, I L, Kumru, B, Liguori, A, Mayr, D, Megdad, E, Meyer, U, Oliveira, R B, Pal, A, Pozzoli, A, Pretese, R, Rocha, J C, Rosenbaum-Fabian, S, Serrano-Nieto, J, Sjoqvist, E, Timmer, C, White, L, van den Hurk, T, van Rijn, M, Zweers, H, Ziadlou, M, MacDonald, A
Published in Orphanet journal of rare diseases (25.01.2018)

by BURTON MICHAEL S, HUNJAN HARJIT S
Year of Publication 18.04.2012