Author response for 'NKX2 .1 run‐on mutation associated to familial brain–lung–thyroid syndrome'

Autor:	Gabriella De Vita, Sara C Credendino, G. Damante, Dario Marin, Paola Cogo, Rosa Gallo, Federica Baldan, Dora Fabbro, Miryam Carecchio, Anna Jolanda Gortan, Elena Cavaliere, Nadia Passon
Rok vydání:	2021
Předmět:	business.industry Brain-Lung-Thyroid Syndrome Mutation (genetic algorithm) Cancer research Medicine business
DOI:	10.1111/cge.13961/v2/response1
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::525ce6ffe7620502a7e3f903801d6deb https://doi.org/10.1111/cge.13961/v2/response1 Zobrazit plný text záznamu