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Authors
Nakajima, Erika
Yokohama, Yuko
Sugiyama, Saori
Taketazu, Mio
Mitsube, Kenrokuro
Yamada, Takahiro
Hammarsjö, Anna
Grigelioniene, Giedre https://orcid.org/0000-0001-9601-3137
Nishimura, Gen
Makita, Yoshio https://orcid.org/0000-0002-0341-5709
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Article History
Received: 26 September 2024
Revised: 9 November 2024
Accepted: 12 November 2024
First Online: 3 December 2024
Ethics approval
: This study was approved by the Institutional Review Board (IRB) of Asahikawa-Kosei General Hospital (no. 2023006) for reporting and by the Regional Ethical Review Board of Karolinska University Hospital and Karolinska Institutet (protocol numbers 2014/983-31/1, 2012/2106-31/4, 2018/2207-32, and 2021-05360) for genomic studies of rare diseases and skeletal dysplasia. Written informed consent for participation in the study and the publication of the patient’s clinical data and images was obtained from the parents.
: The authors declare no competing interests.
