×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
GeneticVariation
CLINVAR
Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling.
27604842
2017
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma.
28738844
2017
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
The phenotype of SDHB germline mutation carriers: a nationwide study.
28490599
2017
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Cardiac Paraganglioma Arising From the Right Atrioventricular Groove in a Paraganglioma-Pheochromocytoma Family Syndrome With Evidence of SDHB Gene Mutation: An Unusual Presentation.
27549546
2016
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma.
27539324
2016
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
GeneticVariation
CLINVAR
Magnetic resonance imaging spectrum of succinate dehydrogenase-related infantile leukoencephalopathy.
26642834
2016
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster Delivery.
26719882
2016
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice.
25695889
2015
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
[Intrapericardical paraganglioma associated with mutation in succinate dehydrogenase enzyme gene].
24939699
2015
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Paraganglioma Presenting as Postpartum Fever of Unknown Origin.
26236513
2015
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathy.
25736212
2015
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
GeneticVariation
CLINVAR
15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5.
26273102
2015
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Succinate Dehydrogenase (SDH)-Deficient Pancreatic Neuroendocrine Tumor Expands the SDH-Related Tumor Spectrum.
26259135
2015
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Superiority of [68Ga]-DOTATATE PET/CT to Other Functional Imaging Modalities in the Localization of SDHB-Associated Metastatic Pheochromocytoma and Paraganglioma.
25873086
2015
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Structural and functional consequences of succinate dehydrogenase subunit B mutations.
25972245
2015
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
SDHD immunohistochemistry: a new tool to validate SDHx mutations in pheochromocytoma/paraganglioma.
25405498
2015
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Association of urinary bladder paragangliomas with germline mutations in the SDHB and VHL genes.
25683602
2015
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
GeneticVariation
CLINVAR
Mitochondrial leukoencephalopathy and complex II deficiency associated with a recessive SDHB mutation with reduced penetrance.
26925370
2015
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Genetics of Apparently Sporadic Pheochromocytoma and Paraganglioma in a Chinese Population.
26267327
2015
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Simultaneous KIT mutation and succinate dehydrogenase (SDH) deficiency in a patient with a gastrointestinal stromal tumour and Carney-Stratakis syndrome: a case report.
25130709
2014
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Phenotype of SDHB mutation carriers in the Netherlands.
25047027
2014
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Clinical exome sequencing for genetic identification of rare Mendelian disorders.
25326637
2014
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Integrative genetic characterization and phenotype correlations in pheochromocytoma and paraganglioma tumours.
24466223
2014
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
Pheochromocytoma and paraganglioma syndromes: genetics and management update.
24523625
2014
×
Entrez Id:
6390
Gene Symbol:
SDHB
SDHB
Pheochromocytoma
0.800
CausalMutation
CLINVAR
SDHB-Associated Paraganglioma in a Pediatric Patient and Literature Review on Hereditary Pheochromocytoma-Paraganglioma Syndromes.
25298897
2014