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Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphisms.
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Document type | Article de périodique (Journal article) – Journal Article, Research Support, Non-U.S. Gov't |
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Access type | Accès restreint |
Publication date | 2011 |
Language | Anglais |
Journal information | "Molecular Genetics and Metabolism" - Vol. 103, no. 3, p. 287-92 (2011) |
Peer reviewed | yes |
Publisher | Academic Press ((United States) Maryland Heights) |
issn | 1096-7192 |
e-issn | 1096-7206 |
Affiliations |
UCL
- (SLuc) Service de rhumatologie UCL - SSS/IREC/RUMA - Pôle de Pathologies rhumatismales |
MESH Subject | Adenosine Triphosphatases - genetics ; Alleles ; Middle Aged ; Osteitis Deformans - genetics ; Polymorphism, Single Nucleotide - genetics ; RANK Ligand - genetics ; Cell Cycle Proteins - genetics ; Female ; Gene Frequency - genetics ; Genetic Predisposition to Disease - genetics ; Haplotypes ; Humans ; Interleukin-6 - genetics ; Male |
Links |
Bibliographic reference | Chung, Pui Yan Jenny ; Beyens, Greet ; de Freitas, Fenna ; Boonen, Steven ; Geusens, Piet ; et. al. Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphisms.. In: Molecular Genetics and Metabolism, Vol. 103, no. 3, p. 287-92 (2011) |
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Permanent URL | http://hdl.handle.net/2078.1/106297 |