Código QR

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts

Abstract Autosomal recessive osteopetrosis (ARO) is a heterogeneous disorder, characterized by defective osteoclastic resorption of bone that results in increased bone density. We have studied nine individuals with an intermediate form of ARO, from the county of Västerbotten in Northern Sweden. All...

Descripción completa

Guardado en:
Autores principales: Eva-Lena Stattin, Petra Henning, Joakim Klar, Emma McDermott, Christina Stecksen-Blicks, Per-Erik Sandström, Therese G. Kellgren, Patrik Rydén, Göran Hallmans, Torsten Lönnerholm, Adam Ameur, Miep H. Helfrich, Fraser P. Coxon, Niklas Dahl, Johan Wikström, Ulf H. Lerner
Formato: Artigo
Lenguaje:Inglês
Publicado: Nature Portfolio 2017-06-01
Colección:Scientific Reports
Acceso en línea:https://doi.org/10.1038/s41598-017-02533-2
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares