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Recessive primary congenital lymphoedema caused by a VEGFR3 mutation
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Document type | Article de périodique (Journal article) – Lettre à l'éditeur |
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Access type | Accès restreint |
Publication date | 2009 |
Journal information | "Journal of Medical Genetics" - Vol. 46, no. 6, p. 399-404 (2009) |
Peer reviewed | yes |
Publisher | B M J Group (London) |
issn | 0022-2593 |
e-issn | 1468-6244 |
Publication status | Publié |
Affiliations |
UCL
- MD/BICL - Département de biochimie et de biologie cellulaire UCL - (SLuc) Centre de malformations vasculaires congénitales UCL - MD/CHIR - Département de chirurgie UCL - (SLuc) Service de chirurgie plastique |
MESH Subject | Vascular Endothelial Growth Factor Receptor-3 - chemistry - genetics - metabolism ; Signal Transduction ; Sequence Alignment ; Pedigree ; Mutation ; Molecular Sequence Data ; Microscopy, Fluorescence ; Lymphedema - congenital - genetics ; Humans ; Genes, Recessive ; Cell Line ; Amino Acid Substitution ; Amino Acid Sequence |
Links |
Bibliographic reference | Ghalamkarpour, Arrask ; Holnthoner, Wolfgang ; Saharinen, Pipsa ; Boon, Laurence M. ; Mulliken, John B. ; et. al. Recessive primary congenital lymphoedema caused by a VEGFR3 mutation. In: Journal of Medical Genetics, Vol. 46, no. 6, p. 399-404 (2009) |
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Permanent URL | http://hdl.handle.net/2078.1/21891 |