Editorial: Rare musculoskeletal disorders: disease mechanisms and therapies

Front Endocrinol (Lausanne). 2023 May 24:14:1215941. doi: 10.3389/fendo.2023.1215941. eCollection 2023.

Authors

Lothar Seefried¹, Nathalie Bravenboer², Erik A Imel³

Affiliations

¹ Department of Osteology, Julius Maximilian University of Würzburg, Würzburg, Germany.
² Department of Clinical Chemistry, Vrije Universiteit Medical Center, Amsterdam University, Amsterdam, Netherlands.
³ Department of Medicine and Pediatrics, Indiana University School of Medicine, Indianapolis, IN, United States.

No abstract available

Keywords: ANO5 gene; X-linked hypophosphataemia (XLH); bone diseases; osteogenesis imperfecta; rare skeletal disorders.

Publication types

Editorial

MeSH terms

Humans
Musculoskeletal Diseases* / therapy
Osteogenesis Imperfecta*