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NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome

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Detalles Bibliográficos
Autores principales:	Cavaliere, Elena, Gortan, Anna Jolanda, Passon, Nadia, Fabbro, Dora, Marin, Dario, Carecchio, Miryam, Baldan, Federica, Credendino, Sara Carmela, Gallo, Rosa, Cogo, Paola, Damante, Giuseppe, De Vita, Gabriella
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Blackwell Publishing Ltd 2021
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8251915/ https://www.ncbi.nlm.nih.gov/pubmed/33778944 http://dx.doi.org/10.1111/cge.13961

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