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

Internet

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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