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Sindrome MEN2 (neoplasia endocrina multipla di tipo 2) : malattia genetica ereditaria che predispone allo sviluppo di tumore midollare della tiroide e di altri tumori endocrini
This results in cardiac chest pain
Specific genetic variants in the GLP1R gene (such as rs6923761) and the FTO gene (rs9939609) can determine whether your body produces enough GLP-1 receptors and how effectively they function
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