A Mutation in TTF1/NKX2.1 Is Associated With Familial Neuroendocrine Cell Hyperplasia of Infancy
Autor: | Young, Lisa R., Deutsch, Gail H., Bokulic, Ronald E., Brody, Alan S., Nogee, Lawrence M. |
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Zdroj: | In Chest October 2013 144(4):1199-1206 |
Databáze: | ScienceDirect |
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