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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
Publikováno v:
BMJ Case Reports; 12/21/2020, Vol. 13, p1-6, 6p