Corrigendum to "Transforming growth factor, beta-2 gene mutation causes autosomal dominant Camurati-Engelmann disease, type 2 (OMIM % 606631)" [Bone 197 (2025) 117477].
Saved in:
| Title: | Corrigendum to "Transforming growth factor, beta-2 gene mutation causes autosomal dominant Camurati-Engelmann disease, type 2 (OMIM % 606631)" [Bone 197 (2025) 117477]. |
|---|---|
| Authors: | Mumm S; Division of Bone and Mineral Diseases, Department of Internal Medicine, Washington University School of Medicine, St Louis, MO 63110, USA; Center for Metabolic Bone Disease and Molecular Research, Shriners Hospitals for Children-St. Louis, St. Louis, MO 63110, USA., Paz-Ibarra JL; Department of Endocrinology, Hospital Nacional Edgardo Rebagliati Martins, Lima, Peru; Department of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru., Campeau PM; Department of Pediatrics, University of Montreal, Montreal, Quebec H3T 1C5, Canada., Garrido-Carrasco E; Department of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru., Baker JC; Musculoskeletal Section, Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO 63110, USA., Pino-Nina E; Department of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru., Duan S; Division of Bone and Mineral Diseases, Department of Internal Medicine, Washington University School of Medicine, St Louis, MO 63110, USA., McAlister WH; Pediatric Radiology Section, Mallinckrodt Institute of Radiology at St. Louis Children's Hospital, Washington University School of Medicine, St. Louis, MO 63110, USA., Whyte MP; Division of Bone and Mineral Diseases, Department of Internal Medicine, Washington University School of Medicine, St Louis, MO 63110, USA; Center for Metabolic Bone Disease and Molecular Research, Shriners Hospitals for Children-St. Louis, St. Louis, MO 63110, USA. Electronic address: mwhyte@wustl.edu. |
| Source: | Bone [Bone] 2025 Nov; Vol. 200, pp. 117573. Date of Electronic Publication: 2025 Aug 06. |
| Publication Type: | Published Erratum |
| Journal Info: | Publisher: Elsevier Science Country of Publication: United States NLM ID: 8504048 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-2763 (Electronic) Linking ISSN: 18732763 NLM ISO Abbreviation: Bone Subsets: MEDLINE; In Process |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
|---|---|
| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 40774839 AccessLevel: 2 PubTypeId: unknown PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Corrigendum to "Transforming growth factor, beta-2 gene mutation causes autosomal dominant Camurati-Engelmann disease, type 2 (OMIM % 606631)" [Bone 197 (2025) 117477]. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Mumm+S%22">Mumm S</searchLink>; Division of Bone and Mineral Diseases, Department of Internal Medicine, Washington University School of Medicine, St Louis, MO 63110, USA; Center for Metabolic Bone Disease and Molecular Research, Shriners Hospitals for Children-St. Louis, St. Louis, MO 63110, USA.<br /><searchLink fieldCode="AU" term="%22Paz-Ibarra+JL%22">Paz-Ibarra JL</searchLink>; Department of Endocrinology, Hospital Nacional Edgardo Rebagliati Martins, Lima, Peru; Department of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru.<br /><searchLink fieldCode="AU" term="%22Campeau+PM%22">Campeau PM</searchLink>; Department of Pediatrics, University of Montreal, Montreal, Quebec H3T 1C5, Canada.<br /><searchLink fieldCode="AU" term="%22Garrido-Carrasco+E%22">Garrido-Carrasco E</searchLink>; Department of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru.<br /><searchLink fieldCode="AU" term="%22Baker+JC%22">Baker JC</searchLink>; Musculoskeletal Section, Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO 63110, USA.<br /><searchLink fieldCode="AU" term="%22Pino-Nina+E%22">Pino-Nina E</searchLink>; Department of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru.<br /><searchLink fieldCode="AU" term="%22Duan+S%22">Duan S</searchLink>; Division of Bone and Mineral Diseases, Department of Internal Medicine, Washington University School of Medicine, St Louis, MO 63110, USA.<br /><searchLink fieldCode="AU" term="%22McAlister+WH%22">McAlister WH</searchLink>; Pediatric Radiology Section, Mallinckrodt Institute of Radiology at St. Louis Children's Hospital, Washington University School of Medicine, St. Louis, MO 63110, USA.<br /><searchLink fieldCode="AU" term="%22Whyte+MP%22">Whyte MP</searchLink>; Division of Bone and Mineral Diseases, Department of Internal Medicine, Washington University School of Medicine, St Louis, MO 63110, USA; Center for Metabolic Bone Disease and Molecular Research, Shriners Hospitals for Children-St. Louis, St. Louis, MO 63110, USA. Electronic address: mwhyte@wustl.edu. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%228504048%22">Bone</searchLink> [Bone] 2025 Nov; Vol. 200, pp. 117573. <i>Date of Electronic Publication: </i>2025 Aug 06. – Name: TypePub Label: Publication Type Group: TypPub Data: Published Erratum – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier+Science%22">Elsevier Science </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>8504048 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1873-2763 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2218732763%22">18732763 </searchLink><i>NLM ISO Abbreviation: </i>Bone <i>Subsets: </i>MEDLINE; In Process |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=40774839 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.bone.2025.117573 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 117573 Titles: – TitleFull: Corrigendum to "Transforming growth factor, beta-2 gene mutation causes autosomal dominant Camurati-Engelmann disease, type 2 (OMIM % 606631)" [Bone 197 (2025) 117477]. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Mumm S – PersonEntity: Name: NameFull: Paz-Ibarra JL – PersonEntity: Name: NameFull: Campeau PM – PersonEntity: Name: NameFull: Garrido-Carrasco E – PersonEntity: Name: NameFull: Baker JC – PersonEntity: Name: NameFull: Pino-Nina E – PersonEntity: Name: NameFull: Duan S – PersonEntity: Name: NameFull: McAlister WH – PersonEntity: Name: NameFull: Whyte MP IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 11 Text: 2025 Nov Type: published Y: 2025 Identifiers: – Type: issn-electronic Value: 1873-2763 Numbering: – Type: volume Value: 200 Titles: – TitleFull: Bone Type: main |
| ResultId | 1 |