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