Associated Papers
Respiratory and other organ manifestations in NKX2-1-related disorders: a systematic review.
Michel K et al.
Frontiers in Medicine, 2025
40395234 (PubMed )
Supplement: Data_Sheet_1.xlsx › Basal_characteristics
Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study.
Elliott AM et al.
Hgg Advances, 2022
35599849 (PubMed )
Supplement: mmc1.xlsx › Sheet1
Deciphering an isolated lung phenotype of NKX2-1 frameshift pathogenic variant.
Delestrain C et al.
Frontiers in Pediatrics, 2022
Heterogeneity of lung disease associated with NK2 homeobox 1 mutations.
Nattes E et al.
Respiratory Medicine, 2017
Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene.
Gras D et al.
Journal of Neurology, Neurosurgery, and Psychiatry, 2012
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