Autosomal recessive mental retardation, deafness, ankylosis, and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous family
Eva Morava, Jirko Kühnisch, Jefte M. Drijvers, Joris H. Robben, Cor Cremers, Petra Van Setten, Amanda Branten, Sabine Stumpp, Alphons De Jong, Krysta Voesenek, Sascha Vermeer, Angelien Heister, Hedi L. Claahsen-Van Der Grinten, Charles W. O'Neill, Michèl A. Willemsen, Dirk Lefeber, Peter M.T. Deen, Uwe Kornak, Hannie Kremer, Ron A. Wevers
Dive into the research topics of 'Autosomal recessive mental retardation, deafness, ankylosis, and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous family'. Together they form a unique fingerprint.