The clinical phenotype of SDHC-associated hebkp_reditary paraganglioma syndrome (PGL3)

Article

Abstract: Context: Mutations in the genes encoding subunits of the succinate dehydrogenase complex cause hebkp

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Autores:

Arts H.A., Else T., Everett J.N., Gruber S.B., Marvin M.L., Raymond V.M., Richard J. Auchus, Stoffel E.M.

Fuentes:

scopus