MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A IN A FAMILY WITH RET C.1901G>A AND NOVEL SLC12A3 MUTATIONS
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DOI: 10.1097/01.hjh.0000837464.81691.1f
Abstract: Objective: In recent years, there has been a lot of controversy about the factors affecting the penetrance of multiple endocrine neoplasia type 2A(MEN2A). Some studies considered it may be related to gene mutations. In the… read more here.
Keywords: men2a; ret 1901g; novel slc12a3; multiple endocrine ... See more keywords
RET c.1901G>A and Novel SLC12A3 Mutations in Familial Pheochromocytomas
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DOI: 10.3390/genes13050864
Abstract: Familial PHEOs (pheochromocytomas) are inherited as an autosomal dominant trait, and inherited PHEOs can be one clinical phenotype of clinical syndromes, such as multiple endocrine neoplasia type 2A (MEN2A). In recent years, there has been… read more here.
Keywords: slc12a3 mutations; ret 1901g; novel slc12a3; pheos ... See more keywords