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Published Erratum
. 2019 Jan;56(1):50-52.
doi: 10.1136/jmedgenet-2017-105127corr1. Epub 2018 Nov 22.

Correction: Tumour risks and genotype-phenotype correlations associated with germline variants in the succinate dehydrogenase subunit genes SDHB, SDHC, and SDHD

No authors listed
Published Erratum

Correction: Tumour risks and genotype-phenotype correlations associated with germline variants in the succinate dehydrogenase subunit genes SDHB, SDHC, and SDHD

No authors listed. J Med Genet. 2019 Jan.
No abstract available

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Figures

Figure 1
Figure 1
Penetrance of for clinically diagnosed disease in proband and non-proband SDHB, SDHC and SDHD mutation carriers with 95% CI shaded. HNPGL, head and neck paraganglioma; PPGL, phaeochromocytoma and paraganglioma.
Figure 2
Figure 2
Penetrance of clinical disease in SDHB mutation carriers by age 60 years, as calculated by different statistical techniques and in different subpopulations. HNPGL, head and neck paraganglioma; PPGL, phaeochromocytoma and paraganglioma; RCC, renal cell carcinoma.
Figure 3
Figure 3
Penetrance of clinical disease in proband and non-proband SDHD p.Pro81Leu mutation carriers versus all other SDHD mutation carriers with 95% CI marked. P values are for the log-rank test comparing the survival distributions of SDHD p.Pro81Leu and all other SDHD mutation carriers. HNPGL, head and neck paraganglioma; PPGL, phaeochromocytoma and paraganglioma.
Figure 4
Figure 4
Supplementary eFigure 4
See this image and copyright information in PMC

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