Osteogenesis imperfecta caused by PPIB mutation with severe phenotype and congenital hearing loss.

Rush, Eric T; Caldwell, Kathleen S; Kreikemeier, Rose M; Lutz, Richard E; Esposito, Paul W.

Afiliación

Rush ET; Department of Pediatrics, University of Nebraska Medical Center, Omaha, NE, USA; Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA; Children's Hospital and Medical Center, Omaha, NE, USA; Munroe-Meyer Institute for Genetics and Rehabilitation, University of Nebra
Caldwell KS; Munroe-Meyer Institute for Genetics and Rehabilitation, University of Nebraska Medical Center, Omaha, NE, USA.
Kreikemeier RM; Children's Hospital and Medical Center, Omaha, NE, USA.
Lutz RE; Department of Pediatrics, University of Nebraska Medical Center, Omaha, NE, USA; Children's Hospital and Medical Center, Omaha, NE, USA; Munroe-Meyer Institute for Genetics and Rehabilitation, University of Nebraska Medical Center, Omaha, NE, USA.
Esposito PW; Department of Pediatrics, University of Nebraska Medical Center, Omaha, NE, USA; Department of Orthopedic Surgery, University of Nebraska Medical Center, Omaha, NE, USA; Children's Hospital and Medical Center, Omaha, NE, USA.

J Pediatr Genet ; 3(1): 29-34, 2014 Mar.

Article en En | MEDLINE | ID: mdl-27625864