Article
Functional consequences of succinate dehydrogenase mutations.
Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists - 1 Jan 2000
Opocher Giuseppe, Schiavi Francesca
Abstract excerpt
UNLABELLED: To explore the genotype-phenotype correlation among the different forms of hereditary paraganglioma. METHODS: We reviewed the pertinent literature on hereditary paragangliomas, which showed the established classification of types 1, 2, 3, and 4 paraganglioma syndrome (PGL1, PGL2, PGL3, and PGL4, respectively). Germline mutations of succinate dehydrogenase confer susceptibilities as follows: SDHD...
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