SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation.

Cascon Soriano, AlbertoCebrián, ARuiz-Llorente, STellería, DBenítez, JRobledo, M2025-01-172025-01-172002-10https://hdl.handle.net/20.500.12105/26061We thank the patients participating in this study and the clinicians who provided blood samples and clinical information. We are also grateful for the technical assistance of Rocio Leton. This work was partially supported by the Fondo de Investigaciones Sanitarias project, FIS 00/0118. Alberto Cascon is a postdoctoral fellow of the Excmo Ayuntamiento de Madrid, Spain.engVoRhttp://creativecommons.org/licenses/by-nc-nd/4.0/COMPLEX-II GENEENDOCRINE NEOPLASIASDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation.Attribution-NonCommercial-NoDerivatives 4.0 International123620463910E64J Med Genethttps://pmc.ncbi.nlm.nih.gov/articles/PMC1734998/pdf/v039p00e64.pdfopen access