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Article

A mutation in TTF1/NKX2.1 is associated with familial neuroendocrine cell hyperplasia of infancy.

Chest - 1 Oct 2013

Young Lisa R, Deutsch Gail H, Bokulic Ronald E, Brody Alan S, Nogee Lawrence M

Abstract excerpt

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 eight other unrelated patients with NEHI were also investigated. METHODS: The proband's lung biopsy specimen (at age...

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Source

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Identifiers

PMID: 23787483
DOI: 10.1378/chest.13-0811
PMCID: PMC3787915

Genes

TTF1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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