对《53例日本成骨不全患者采用靶向新一代测序技术进行的综合基因分析及基因型-表型相关性研究》的更正
Correction to: Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta.
作者信息
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
机构信息
Department of Pediatrics, Osaka University Graduate School of Medicine, Suita, Japan.
The Japan Environment and Children's Study, Osaka Unit Center, Suita, Japan.
出版信息
Osteoporos Int. 2020 Jun;31(6):1185. doi: 10.1007/s00198-020-05396-y.
Abstract
The original article has been corrected.
摘要
原文已被修正。
相似文献
1
Correction to: Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta.对《53例日本成骨不全患者采用靶向新一代测序技术进行的综合基因分析及基因型-表型相关性研究》的更正
Osteoporos Int. 2020 Jun;31(6):1185. doi: 10.1007/s00198-020-05396-y.
2
Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta.53 例日本成骨不全症患者的靶向下一代测序综合遗传学分析及基因型-表型相关性。
Osteoporos Int. 2019 Nov;30(11):2333-2342. doi: 10.1007/s00198-019-05076-6. Epub 2019 Jul 29.
3
Gene mutation spectrum and genotype-phenotype correlation in a cohort of Chinese osteogenesis imperfecta patients revealed by targeted next generation sequencing.通过靶向下一代测序揭示中国成骨不全症患者的基因突变谱和基因型-表型相关性。
Osteoporos Int. 2017 Oct;28(10):2985-2995. doi: 10.1007/s00198-017-4143-8. Epub 2017 Jul 19.
4
Correction to: Gene mutation spectrum and genotype-phenotype correlation in a cohort of Chinese osteogenesis imperfecta patients revealed by targeted next generation sequencing.
Osteoporos Int. 2018 Jan;29(1):261. doi: 10.1007/s00198-017-4250-6.
5
Genotype-phenotype analysis of a rare type of osteogenesis imperfecta in four Chinese families with WNT1 mutations.四个携带WNT1基因突变的中国家庭中罕见型成骨不全症的基因型-表型分析
Clin Chim Acta. 2016 Oct 1;461:172-80. doi: 10.1016/j.cca.2016.07.012. Epub 2016 Jul 20.
6
[Phenotype-genotype analysis and detection of gene variant in six families with osteogenesis imperfecta].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 May 10;37(5):514-518. doi: 10.3760/cma.j.issn.1003-9406.2020.05.005.
7
Two novel distinct COL1A2 mutations highlight the complexity of genotype-phenotype correlations in osteogenesis imperfecta and related connective tissue disorders.两种新的不同的COL1A2突变凸显了成骨不全症及相关结缔组织疾病中基因型-表型相关性的复杂性。
Eur J Med Genet. 2013 Dec;56(12):669-73. doi: 10.1016/j.ejmg.2013.10.002. Epub 2013 Oct 17.
8
Genotype-phenotype correlation among Malaysian patients with osteogenesis imperfecta.马来西亚成骨不全症患者的基因型-表型相关性。
Clin Chim Acta. 2018 Sep;484:141-147. doi: 10.1016/j.cca.2018.05.048. Epub 2018 May 25.
9
Genotype-phenotype relationship in a large cohort of osteogenesis imperfecta patients with COL1A1 mutations revealed by a new scoring system.通过新的评分系统揭示 COL1A1 突变的大型成骨不全症患者的基因型-表型关系。
Chin Med J (Engl). 2019 Jan 20;132(2):145-153. doi: 10.1097/CM9.0000000000000013.
10
Osteogenesis imperfecta types I-XI: implications for the neonatal nurse.Ⅰ至Ⅺ型成骨不全症：对新生儿护士的启示
Adv Neonatal Care. 2014 Oct;14(5):309-15; quiz 316-7. doi: 10.1097/ANC.0000000000000094.
引用本文的文献
1
Scoliosis in osteogenesis imperfecta: identifying the genetic and non-genetic factors affecting severity and progression from longitudinal data of 290 patients.成骨不全症中的脊柱侧凸：从 290 名患者的纵向数据中确定影响严重程度和进展的遗传和非遗传因素。
Orphanet J Rare Dis. 2023 Sep 20;18(1):295. doi: 10.1186/s13023-023-02906-z.
2
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.骨小梁骨评分和骨矿表观密度与成骨不全症患儿和青少年骨脆弱性严重程度的相关性：一项横断面研究。
PLoS One. 2023 Aug 29;18(8):e0290812. doi: 10.1371/journal.pone.0290812. eCollection 2023.
Zotero 插件