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Updated: Jan 4, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Haploinsufficiency of NKX2-1 in Brain-Lung-Thyroid Syndrome with Additional Multiple Pituitary Dysfunction

Rathi Prasad1, Adeline K Nicholas2, Nadia Schoenmakers2

  • 1Department of Paediatric Endocrinology, Royal London Hospital, Barts Health NHS Trust, London, United Kingdom, Rathi.Prasad@nhs.net.

Hormone Research in Paediatrics
|November 11, 2019
PubMed
Abstract

Keywords:
Brain-lung-thyroid syndromeCongenital hypothyroidismHypopituitarismNKX2-1

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