Multiple epiphyseal dysplasia: A clinical and genetic study of 12 cases in a Swedish 6-generation family

por Dahlqvist, Johanna, Örlén, Hanna, Matsson, Hans, Dahl, Niklas, LÖnnerholm, Torsten, Gustavson, Karl-Henrik
Publicado 2009

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts

por Stattin, Eva-Lena, Henning, Petra, Klar, Joakim, McDermott, Emma, Stecksen-Blicks, Christina, Sandström, Per-Erik, Kellgren, Therese G., Rydén, Patrik, Hallmans, Göran, Lönnerholm, Torsten, Ameur, Adam, Helfrich, Miep H., Coxon, Fraser P., Dahl, Niklas, Wikström, Johan, Lerner, Ulf H.
Publicado 2017