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pro vyhledávání: '"Bernardo Conde Maria"'
Publikováno v:
BMJ Case Reports
Type 1 multiple endocrine neoplasia (MEN-1) syndrome is an autosomal dominant disease, associated with germline mutations in the MEN-1 tumour suppressor gene (encoding the menin protein). Recent studies, through a better characterisation of the funct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6451391b3285c53325733793f39687a0
https://doi.org/10.1136/bcr-2020-238784
https://doi.org/10.1136/bcr-2020-238784
