Journal Article
Morava, E.; Kuhnisch, J.; Drijvers, J. M.; Robben, J. H.; Cremers, C.; van Setten, P.; Branten, A.; Stumpp, S.; de Jong, A.; Voesenek, K. et al.; Vermeer, S.; Heister, A.; Claahsen-van der Grinten, H. L.; O'Neill, C. W.; Willemsen, M. A.; Lefeber, D.; Deen, P. M.; Kornak, U.; Kremer, H.; Wevers, R. A.: Autosomal recessive mental retardation, deafness, ankylosis, and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous family. J Clin Endocrinol Metab
96 (1), pp. E189 - 98 (2011)