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Updated: May 14, 2026

06:41
In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Novel NKX2.1 mutation associated with hypothyroidism and lethal respiratory failure in a full-term neonate
E S Gillett1, G H Deutsch, M J Bamshad
1Department of Pediatrics, Division of Neonatology, University of Washington School of Medicine, Seattle Children's Hospital, Seattle, WA 98105, USA.
Abstract:
We report a case of lethal neonatal hypoxic respiratory failure and hypothyroidism in an infant with a novel missense mutation in NKX2.1.
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