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:
Bibliographic Details
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