Atypical type VI Osteogenesis Imperfecta mouse models the intersection of IFITM5 and SERPINF1 pathways in patients
Gali Guterman-Ram,
Ghazal Hedjazi,
Chris Stephan,
Stéphane Blouin,
Jochen Zwerina,
Kenneth M. Kozloff,
Nadja Fratzl-Zelman,
Joan C. Marini
Affiliations
Gali Guterman-Ram
Eunice Kennedy Shriver National Institute of Child Health and Human Development- National Institutes of Health, Section on Heritable Disorders of Bone and Extracellular Matrix, Bethesda, United States; Corresponding author.
Ghazal Hedjazi
Hanusch Hospital of OEGK and AUVA Trauma Centre Meidling- 1st Med. Dept. Hanusch Hospital, Ludwig Boltzmann Institute of Osteology, Vienna, Austria
Chris Stephan
University of Michigan, Departments of Orthopaedic Surgery and Biomedical Engineering, Ann Arbor, United States
Stéphane Blouin
Hanusch Hospital of OEGK and AUVA Trauma Centre Meidling- 1st Med. Dept. Hanusch Hospital, Ludwig Boltzmann Institute of Osteology, Vienna, Austria
Jochen Zwerina
Hanusch Hospital of OEGK and AUVA Trauma Centre Meidling- 1st Med. Dept. Hanusch Hospital, Ludwig Boltzmann Institute of Osteology, Vienna, Austria
Kenneth M. Kozloff
University of Michigan, Departments of Orthopaedic Surgery and Biomedical Engineering, Ann Arbor, United States
Nadja Fratzl-Zelman
Hanusch Hospital of OEGK and AUVA Trauma Centre Meidling- 1st Med. Dept. Hanusch Hospital, Ludwig Boltzmann Institute of Osteology, Vienna, Austria
Joan C. Marini
Eunice Kennedy Shriver National Institute of Child Health and Human Development- National Institutes of Health, Section on Heritable Disorders of Bone and Extracellular Matrix, Bethesda, United States
