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

BACKGROUND: Neuroendocrine cell hyperplasia of infancy (NEHI) is a childhood diffuse lung disease of unknown etiology. We investigated the mechanism for lung disease in a subject whose clinical, imaging, and lung biopsy specimen findings were consistent with NEHI; the subject’s extended family and e...

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Main Authors: Young, Lisa R., Deutsch, Gail H., Bokulic, Ronald E., Brody, Alan S., Nogee, Lawrence M.
Format: Artigo
Jezik:Inglês
Izdano: American College of Chest Physicians 2013
Teme:
Original Research
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3787915/
https://ncbi.nlm.nih.gov/pubmed/23787483
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1378/chest.13-0811
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