Editorial: Rare musculoskeletal disorders: disease mechanisms and therapies

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fendo-14-1215941.pdf (247.5 KB)
Date
2023-05-24
Authors
Seefried, Lothar
Bravenboer, Nathalie
Imel, Erik A.
Language
American English
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Medicine, School of Medicine
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Frontiers Media
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ANO5 gene, X-linked hypophosphataemia (XLH), Bone diseases, Osteogenesis imperfecta, Rare skeletal disorders
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Cite As
Seefried L, Bravenboer N, Imel EA. Editorial: Rare musculoskeletal disorders: disease mechanisms and therapies. Front Endocrinol (Lausanne). 2023;14:1215941. Published 2023 May 24. doi:10.3389/fendo.2023.1215941
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Frontiers in Endocrinology
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https://hdl.handle.net/1805/38180
DOI
https://doi.org/10.3389/fendo.2023.1215941
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Final published version
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