A Mutation in TTF1 / NKX2.1 Is Associated With Familial Neuroendocrine Cell Hyperplasia of Infancy

Title
A Mutation in TTF1 / NKX2.1 Is Associated With Familial Neuroendocrine Cell Hyperplasia of Infancy
Authors
Keywords
-
Journal
CHEST
Volume 144, Issue 4, Pages 1199-1206
Publisher
Elsevier BV
Online
2013-06-20
DOI
10.1378/chest.13-0811

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