Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase - Concepedia

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Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase

DOI Full Paper Access

433

Citations

18

References

2000

Year

Alexandre Irrthum, Marika J. Karkkainen, Koenraad Devriendt, Kari Alitalo, Miikka Vikkula

The American Journal of Human Genetics

Developmental BiologyGenetic DisorderImmunologyPathologyFibroblast Growth FactorLymphatic DiseaseVegfr3 Tyrosine KinaseSclerodermaMedicineCongenital Hereditary Lymphedema

References

	Year	Citations

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