NKX2.1 run-on mutation associated to familial brain-lung-thyroid syndrome.
Cavaliere E, Gortan AJ, Passon N, Fabbro D, Marin D, Carecchio M, Baldan F, Credendino SC, Gallo R, Cogo P, Damante G, De Vita G.
Cavaliere E, et al. Among authors: cogo p.
Clin Genet. 2021 Jul;100(1):114-116. doi: 10.1111/cge.13961. Epub 2021 Mar 29.
Clin Genet. 2021.
PMID: 33778944
Free PMC article.