Correction to: Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta

Y Ohata¹, S Takeyari¹, Y Nakano¹, T Kitaoka¹, H Nakayama^{1

2}, V Bizaoui^{1

3}, K Yamamoto^{1

4}, K Miyata¹, K Yamamoto^{1

5}, M Fujiwara^{1

6}, T Kubota¹, T Michigami⁷, K Yamamoto⁸, T Yamamoto⁹, N Namba^{1

10}, K Ebina¹¹, H Yoshikawa¹², K Ozono¹³

Affiliations

¹ Department of Pediatrics, Osaka University Graduate School of Medicine, Suita, Japan.
² The Japan Environment and Children's Study, Osaka Unit Center, Suita, Japan.
³ Department of Medical Genetics, Reference Center for Skeletal Dysplasia, Hôpital Necker - Enfants Malades, Paris, France.
⁴ Department of Statistical Genetics, Osaka University Graduate School of Medicine, Suita, Japan.
⁵ Department of Pediatrics, National Hospital Organization Osaka National Hospital, Osaka, Japan.
⁶ The First Department of Oral and Maxillofacial Surgery, Osaka University Graduate School of Dentistry, Suita, Japan.
⁷ Department of Bone and Mineral Research, Osaka Women's and Children's Hospital, Izumi, Japan.
⁸ Department of Pediatric Nephrology and Metabolism, Osaka Women's and Children's Hospital, Izumi, Japan.
⁹ Department of Pediatrics, Minoh City Hospital, Minoh, Japan.
¹⁰ Department of Pediatrics, Osaka Hospital, Japan Community Healthcare Organization (JCHO), Osaka, Japan.
¹¹ Department of Musculoskeletal Regenerative Medicine, Osaka University Graduate School of Medicine, Suita, Japan.
¹² Department of Orthopaedic Surgery, Osaka University Graduate School of Medicine, Suita, Japan.
¹³ Department of Pediatrics, Osaka University Graduate School of Medicine, Suita, Japan. keioz@ped.med.osaka-u.ac.jp.

PMID: 32246166
PMCID: PMC7237517
DOI: 10.1007/s00198-020-05396-y

Published Erratum

Correction to: Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta

Y Ohata et al. Osteoporos Int. 2020 Jun.

. 2020 Jun;31(6):1185.

doi: 10.1007/s00198-020-05396-y.

Authors

Affiliations

¹ Department of Pediatrics, Osaka University Graduate School of Medicine, Suita, Japan.
² The Japan Environment and Children's Study, Osaka Unit Center, Suita, Japan.
³ Department of Medical Genetics, Reference Center for Skeletal Dysplasia, Hôpital Necker - Enfants Malades, Paris, France.
⁴ Department of Statistical Genetics, Osaka University Graduate School of Medicine, Suita, Japan.
⁵ Department of Pediatrics, National Hospital Organization Osaka National Hospital, Osaka, Japan.
⁶ The First Department of Oral and Maxillofacial Surgery, Osaka University Graduate School of Dentistry, Suita, Japan.
⁷ Department of Bone and Mineral Research, Osaka Women's and Children's Hospital, Izumi, Japan.
⁸ Department of Pediatric Nephrology and Metabolism, Osaka Women's and Children's Hospital, Izumi, Japan.
⁹ Department of Pediatrics, Minoh City Hospital, Minoh, Japan.
¹⁰ Department of Pediatrics, Osaka Hospital, Japan Community Healthcare Organization (JCHO), Osaka, Japan.
¹¹ Department of Musculoskeletal Regenerative Medicine, Osaka University Graduate School of Medicine, Suita, Japan.
¹² Department of Orthopaedic Surgery, Osaka University Graduate School of Medicine, Suita, Japan.
¹³ Department of Pediatrics, Osaka University Graduate School of Medicine, Suita, Japan. keioz@ped.med.osaka-u.ac.jp.

PMID: 32246166
PMCID: PMC7237517
DOI: 10.1007/s00198-020-05396-y

Abstract

The original article has been corrected.

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Erratum for

Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta.
Ohata Y, Takeyari S, Nakano Y, Kitaoka T, Nakayama H, Bizaoui V, Yamamoto K, Miyata K, Yamamoto K, Fujiwara M, Kubota T, Michigami T, Yamamoto K, Yamamoto T, Namba N, Ebina K, Yoshikawa H, Ozono K. Ohata Y, et al. Osteoporos Int. 2019 Nov;30(11):2333-2342. doi: 10.1007/s00198-019-05076-6. Epub 2019 Jul 29. Osteoporos Int. 2019. PMID: 31363794 Free PMC article.

Cited by

Scoliosis in osteogenesis imperfecta: identifying the genetic and non-genetic factors affecting severity and progression from longitudinal data of 290 patients.
Chen P, Zhou Y, Tan Z, Lin Y, Lin DL, Wu J, Li Z, Shek HT, Wu J, Hu Y, Zhu F, Chan D, Cheung KM, To MK. Chen P, et al. Orphanet J Rare Dis. 2023 Sep 20;18(1):295. doi: 10.1186/s13023-023-02906-z. Orphanet J Rare Dis. 2023. PMID: 37730650 Free PMC article.
Association of trabecular bone score and bone mineral apparent density with the severity of bone fragility in children and adolescents with osteogenesis imperfecta: A cross-sectional study.
Ohata Y, Kitaoka T, Ishimi T, Yamada C, Nakano Y, Yamamoto K, Takeyari S, Nakayama H, Fujiwara M, Kubota T, Ozono K. Ohata Y, et al. PLoS One. 2023 Aug 29;18(8):e0290812. doi: 10.1371/journal.pone.0290812. eCollection 2023. PLoS One. 2023. PMID: 37643181 Free PMC article.

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Correction to: Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta

Affiliations

Correction to: Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta

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