The Clinical Phenotype of SDHC-Associated Hereditary Paraganglioma Syndrome (PGL3)

CONTEXT: Mutations in the genes encoding subunits of the succinate dehydrogenase complex cause hereditary paraganglioma syndromes. Although the phenotypes associated with the more commonly mutated genes, SDHB and SDHD, are well described, less is known about SDHC-associated paragangliomas. OBJECTIVE...

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Xehetasun bibliografikoak
Egile Nagusiak: Else, Tobias, Marvin, Monica L., Everett, Jessica N., Gruber, Stephen B., Arts, H. Alexander, Stoffel, Elena M., Auchus, Richard J., Raymond, Victoria M.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Endocrine Society 2014
Gaiak:
JCEM Online: Advances in Genetics
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4121019/
https://ncbi.nlm.nih.gov/pubmed/24758179
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2013-3853
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