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Identification of Association of Common AGGF1Variants with Susceptibility for Klippel-Trenaunay Syndrome Using the Structure Association Program
Klippel-Trenaunay syndrome (KTS) is a severe congenital disorder characterized by capillary malformations, venous malformations or varicose veins, and hypertrophy of the affected tissues. The angiogenic factor gene AGGF1 was previously identified as a candidate susceptibility gene for KTS, but furth...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2008
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2602961/ https://ncbi.nlm.nih.gov/pubmed/18564129 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-1809.2008.00458.x |
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