Associated Papers
High incidence of occult familial SDHD cases amongst Czech patients with head and neck paragangliomas.
Guha A et al.
Frontiers in Endocrinology, 2023
Quantifying evidence toward pathogenicity for rare phenotypes: The case of succinate dehydrogenase genes, SDHB and SDHD.
Garrett A et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2022
34906457 (PubMed )
Supplement: mmc1.xlsx › SupTable2_Variant_Counts
Consolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiency.
Lin S et al.
European Journal of Human Genetics : Ejhg, 2021
34012134 (PubMed )
Supplement: 41431_2021_887_MOESM1_ESM.docx
Mutation Frequency in Main Susceptibility Genes Among Patients With Head and Neck Paragangliomas.
Snezhkina AV et al.
Frontiers in Genetics, 2020
33391357 (PubMed )
Supplement: Data_Sheet_1.PDF
Exome analysis of carotid body tumor.
Snezhkina AV et al.
Bmc Medical Genomics, 2018
29504908 (PubMed )
Supplement: 12920_2018_327_MOESM3_ESM.xlsx › s2
In Vivo Detection of Succinate by Magnetic Resonance Spectroscopy as a Hallmark of SDHx Mutations in Paraganglioma.
Lussey-Lepoutre C et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2016
[Myocardial calcinosis in a juvenile patient with Wermer syndrome (multiple endocrine neoplasia type I)].
Stefenelli T et al.
Wiener Klinische Wochenschrift, 1992
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