Neonatal High Bone Mass With First Mutation of the NF-κB Complex: Heterozygous De Novo Missense (p.Asp512Ser)RELA(Rela/p65)

Author:

Frederiksen Anja L12,Larsen Martin J12,Brusgaard Klaus12,Novack Deborah V3,Knudsen Peter Juel Thiis4,Schrøder Henrik Daa5,Qiu Weimin6,Eckhardt Christina7,McAlister William H8,Kassem Moustapha6,Mumm Steven39,Frost Morten10,Whyte Michael P39

Affiliation:

1. Department of Clinical Genetics; Odense University Hospital; Odense Denmark

2. Human Genetics; Institute of Clinical Research; University of Southern Denmark; Odense Denmark

3. Division of Bone and Mineral Diseases; Washington University School of Medicine at Barnes-Jewish Hospital; St. Louis MO USA

4. Institute of Forensic Medicine; University of Southern Denmark; Odense Denmark

5. Department of Pathology; Odense University Hospital; Odense Denmark

6. Molecular Endocrinology Laboratory (KMEB); Department of Endocrinology; Odense University Hospital and University of Southern Denmark; Odense Denmark

7. Department of Pediatrics; Odense University Hospital; Odense Denmark

8. Department of Pediatric Radiology; Mallinckrodt Institute of Radiology; Washington University School of Medicine at St. Louis Children's Hospital; St. Louis MO USA

9. Center for Metabolic Bone Disease and Molecular Research; Shriners Hospital for Children; St. Louis MO USA

10. Endocrine Research Unit; Odense University Hospital; Odense Denmark

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

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