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Milroy disease and the VEGFR-3 mutation phenotype
Primary congenital lymphoedema (Milroy disease) is a rare autosomal dominant condition for which a major causative gene defect has recently been determined. Mutations in the vascular endothelial growth factor receptor 3 (VEGFR-3) gene have now been described in 13 families world-wide. This is a revi...
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| Hauptverfasser: | , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMJ Group
2005
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1735984/ https://ncbi.nlm.nih.gov/pubmed/15689446 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.024802 |
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