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...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Brice, G, Child, A, Evans, A, Bell, R, Mansour, S, Burnand, K, Sarfarazi, M, Jeffery, S, Mortimer, P
Format: Artigo
Sprog:Inglês
Udgivet: BMJ Group 2005
Fag:
Review
Online adgang: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
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker