FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.
| Autor: | Kriederman, Benjamin M., Myloyde, Teressa L., Witte, Marlys H., Dagenais, Susan L., Witte, Charles L., Rennels, Margaret, Bernas, Michael J., Lynch, Michelle T., Erickson, Robert P., Caulder, Mark S., Miura, Naoyuki, Jackson, David, Brooks, Brian P., Glover, Thomas W. |
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| Zdroj: | Human Molecular Genetics; May2003, Vol. 12 Issue 10, p1179-1185, 7p |
| Databáze: | Complementary Index |
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