Progressive skeletal defects caused by Kindlin3 deficiency, a model of autosomal recessive osteopetrosis in humans.

Autor: Dudiki T; Department of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA., Nascimento DW; Department of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA., Childs LS; Department of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA., Kareti S; Department of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA., Androjna C; Biomedical Engineering, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA., Zhevlakova I; Department of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA., Byzova TV; Department of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA. Electronic address: byzovat@ccf.org.

Publikováno v: Bone [Bone] 2022 Jul; Vol. 160, pp. 116397. Date of Electronic Publication: 2022 Mar 25.