Bone tissue and osteoblasts from X-linked type XVIII OI with defects in regulated intramembrane proteolysis have distinct features

• Allahdad Zarei,
• Nadja Fratzl-Zelman,
• An Dang Do,
• Megan Glassford,
• Mark Hannibal,
• Maegan Wallace,
• Paul W. Esposito,
• Kristin Lindstrom,
• Jochen Zwerina,
• Marianne Knue,
• Sara Talvacchio,
• Joan.C. Marini

Affiliations

Allahdad Zarei

NICHD-NIH, Section on Heritable Disorders of Bone and Extracellular MatrixB, Bethesda, United States; Corresponding author.

Nadja Fratzl-Zelman

Hanusch Hospital, Ludwig Boltzmann Institute of Osteology, Vienna, Austria

An Dang Do

NICHD-NIH, Office of Clinical Director, Bethesda, United States

Megan Glassford

University of Michigan Medical School, Department of Pediatrics and Communicable Diseases, Ann Arbor, United States

Mark Hannibal

University of Michigan Medical School, Department of Pediatrics and Communicable Diseases, Ann Arbor, United States

Maegan Wallace

University of Nebraska Medical Center, Department of Orthopaedic Surgery, Omaha, United States

Paul W. Esposito

University of Nebraska Medical Center, Department of Orthopaedic Surgery, Omaha, United States

Kristin Lindstrom

Phoenix Childern’s Hospital-Main, Division of Genetics and Metabolism, Phoenix, United States

Jochen Zwerina

Hanusch Hospital, Ludwig Boltzmann Institute of Osteology, Vienna, Austria

Marianne Knue

NICHD-NIH, Office of Clinical Director, Bethesda, United States

Sara Talvacchio

NICHD-NIH, Office of Clinical Director, Bethesda, United States

Joan.C. Marini

NICHD-NIH, Section on Heritable Disorders of Bone and Extracellular Matrix, Bethesda, United States