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.
Zdroj: In Chest October 2013 144(4):1199-1206
Databáze: ScienceDirect