Associated Papers
NKX2-1 gene variants in solid tumours: the spectrum of gene variants and potential impact in surgical pathology diagnosis.
Yoon JY et al.
Journal of Clinical Pathology, 2025
Mutational and bioinformatics analysis of the NKX2.1 gene in a cohort of Iranian pediatric patients with congenital hypothyroidism (CH).
Heidari MM et al.
Physiology International, 2022
Altered pituitary morphology as a sign of benign hereditary chorea caused by TITF1/NKX2.1 mutations.
Thust S et al.
Neurogenetics, 2022
NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement.
Balicza P et al.
Frontiers in Genetics, 2018
NKX2.1-Related Disorders: a novel mutation with mild clinical presentation.
Monti S et al.
Italian Journal of Pediatrics, 2015
Benign Hereditary Chorea: An Update.
Peall KJ et al.
Tremor and Other Hyperkinetic Movements (new York, N.y.), 2015
Benign hereditary chorea related to NKX2.1: expansion of the genotypic and phenotypic spectrum.
Peall KJ et al.
Developmental Medicine and Child Neurology, 2014
Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum.
Thorwarth A et al.
Journal of Medical Genetics, 2014
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