Persistent lung disease in adults with NKX2.1 mutation and familial neuroendocrine cell hyperplasia of infancy

Rebekah J. Nevel, Errine T. Garnett, John A. Worrell, Ronald L. Morton, Lawrence M. Nogee, Timothy S. Blackwell, Lisa R. Young

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Fingerprint

Dive into the research topics of 'Persistent lung disease in adults with NKX2.1 mutation and familial neuroendocrine cell hyperplasia of infancy'. Together they form a unique fingerprint.

Medicine & Life Sciences