Common and recurrent HPGD mutations in Caucasian individuals with primary hypertrophic osteoarthropathy
- Autor
- DIGGLE, Christine P1 ; CARR, Ian M1 ; BONTHRON, David T1 ; ZITT, Emanuel2 ; WUSIK, Katie3 ; HOPKIN, Robert J3 ; PRADA, Carlos E3 ; CALABRESE, Olga4 ; RITTINGER, Olaf5 ; PUNARO, Marilynn G6 ; MARKHAM, Alexander F1
[1] Leeds Institute of Molecular Medicine, University of Leeds, St James's University Hospital, Leeds, United Kingdom
[2] Department of Nephrology and Dialysis, Landeskrankenhaus Feldkirch, Academic Teaching Hospital of Innsbruck Medical University, Feldkirch-Tisis, Austria
[3] Division of Human Genetics, Cincinnati Children's Hospital, Cincinnati, OH, United States
[4] Servizio di Genetica Medica, St Anna Hospital, Ferrara, Italy
[5] Clinical Genetics Unit, Paracelsus Medical University, General Hospital of Salzburg, Salzburg, Austria
[6] Division of Pediatric Rheumatology, University of Texas Southwestern Medical Center, Texas Scottish Rite Hospital, Dallas, TX, United States - Fuente
Rheumatology (Oxford. Print). 2010, Vol 49, Num 6, pp 1056-1062, 7 p ; ref : 15 ref
- ISSN
- 1462-0324
- Campo Científico
- Rheumatology
- Editor
- Oxford University Press, Oxford
- País de la publicación
- United Kingdom
- Tipo de documento
- Article
- Idioma
- English
- Palabra clave de autor
- 15-hydroxyprostaglandin dehydrogenase Clubbing Primary hypertrophic osteoarthropathy Prostaglandin
- Palabra clave (fr)
- Homme Mutation Pachydermopériostose Prostaglandine Rhumatologie Récidive Maladie héréditaire Ostéochondrodysplasie Pathologie de la peau Pathologie du système ostéoarticulaire
- Palabra clave (in)
- Human Mutation Pachydermoperiostosis Prostaglandin Rheumatology Relapse Genetic disease Osteochondrodysplasia Skin disease Diseases of the osteoarticular system
- Palabra clave (es)
- Hombre Mutación Paquidermoperiostosis Prostaglandina Reumatología Recaida Enfermedad hereditaria Osteocondrodisplasia Piel patología Sistema osteoarticular patología
- Clasificación
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B15 Diseases of the osteoarticular system / 002B15H Malformations and congenital and or hereditary diseases involving bones. Joint deformations
- Disciplina
- Osteoarticular pathology
- Procedencia
- Inist-CNRS
- Base de datos
- PASCAL
- Identificador INIST
- 22829410
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1093/rheumatology/keq048 
https://dx.doi.org/10.1093/rheumatology/keq048
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