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Autor:
F J, Pomares Gómez, M J, Bernabé Espinosa, X, Matías-Guiu Guía, J M, Rodríguez González, J, Soriano Palao, J, Sola Pérez, P, Carbonell Meseguer, P, Parrilla Paricio, F J, Tébar Massó
Publikováno v:
Medicina clinica. 112(17)
Multiple endocrine neoplasia type 2 (MEN 2) syndromes are inherited following an autosomal dominant pattern. RET protooncogen mutations have been associated with MEN 2. The identification of these mutations enables us to diagnose MEN 2. The objective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::07c3e1a9282d2fbc3757cdaa90e20f28
https://pubmed.ncbi.nlm.nih.gov/10374185
https://pubmed.ncbi.nlm.nih.gov/10374185
