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Transforming growth factor, beta-2 gene mutation causes autosomal dominant Camurati-Engelmann disease, type 2 (OMIM % 606631).

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Title: Transforming growth factor, beta-2 gene mutation causes autosomal dominant Camurati-Engelmann disease, type 2 (OMIM % 606631).
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. Electronic address: smumm@wustl.edu., Paz-Ibarra JL; Department of Endocrinology, Hospital Nacional Edgardo Rebagliati Martins, Lima, Peru; Department of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru. Electronic address: jose.paz1@unmsm.edu.pe., Campeau PM; Department of Pediatrics, University of Montreal, Montreal, Quebec H3T 1C5, Canada. Electronic address: p.campeau@umontreal.ca., 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. Electronic address: jonathancbaker@wustl.edu., 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. Electronic address: sduan@wustl.edu., 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. Electronic address: mcalisterw@wustl.edu., 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 Aug; Vol. 197, pp. 117477. Date of Electronic Publication: 2025 Apr 07.
Publication Type: Journal Article; Case Reports
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
Database: MEDLINE Ultimate
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  Data: Transforming growth factor, beta-2 gene mutation causes autosomal dominant Camurati-Engelmann disease, type 2 (OMIM % 606631).
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  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. Electronic address: smumm@wustl.edu.<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. Electronic address: jose.paz1@unmsm.edu.pe.<br /><searchLink fieldCode="AU" term="%22Campeau+PM%22">Campeau PM</searchLink>; Department of Pediatrics, University of Montreal, Montreal, Quebec H3T 1C5, Canada. Electronic address: p.campeau@umontreal.ca.<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. Electronic address: jonathancbaker@wustl.edu.<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. Electronic address: sduan@wustl.edu.<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. Electronic address: mcalisterw@wustl.edu.<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.
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  Data: <searchLink fieldCode="JN" term="%228504048%22">Bone</searchLink> [Bone] 2025 Aug; Vol. 197, pp. 117477. <i>Date of Electronic Publication: </i>2025 Apr 07.
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  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
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        Value: 10.1016/j.bone.2025.117477
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        Text: English
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              Text: 2025 Aug
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