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pro vyhledávání: '"Kraus, Mh H."'
Autor:
Santoro, M., Carlomagno, F., Romano, A., Bottaro, Dp P., Dathan, Na A., Grieco, M., Fusco, A., Vecchio, G., Matoskova, B., Kraus, Mh H., Di Fiore, P. P., Difiore, Pp, Et, A.
Multiple endocrine neoplasia types 2A and 2B (MEN2A and MEN2B) and familial medullary thyroid carcinoma are dominantly inherited cancer syndromes. All three syndromes are associated with mutations in RET, which encodes a receptor-like tyrosine kinase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::3a4763b8637d995fcbbebc531db77066
https://zenodo.org/record/894824
https://zenodo.org/record/894824
