Associated Papers
Deciphering the pathogenicity of three NKX2-1 variants in ultra-severe forms of childhood interstitial lung disease.
Soreze YD et al.
Plos One, 2025
The First Indian Patient With Benign Hereditary Chorea due to a De Novo Mutation in the NKX2-1 Gene.
Garg D et al.
Journal of Movement Disorders, 2024
Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism.
Li M et al.
International Journal of Molecular Sciences, 2023
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