HGF and MET Mutations in Primary and Secondary Lymphedema

Background: Lymphedema is the abnormal accumulation of protein-rich fluid in the interstitial space. Primary lymphedema is a rare genetic condition with both autosomal dominant and autosomal recessive modes of inheritance. Three genes, FLT4 (VEGFR3), FOXC2, and SOX18 cause varying forms of primary l...

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Bibliografske podrobnosti
izdano v:Lymphat Res Biol
Main Authors: Finegold, David N., Schacht, Vivien, Kimak, Mark A., Lawrence, Elizabeth C., Foeldi, Etelka, Karlsson, Jenny M., Baty, Catherine J., Ferrell, Robert E.
Format: Artigo
Jezik:Inglês
Izdano: Mary Ann Liebert, Inc. 2008
Teme:
Original Papers
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4298750/
https://ncbi.nlm.nih.gov/pubmed/18564920
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/lrb.2008.1524
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