Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD.
|
29386252 |
2018 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers.
|
28503760 |
2018 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
GeneticVariation |
CLINVAR |
The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers.
|
28503760 |
2018 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
The phenotype of SDHB germline mutation carriers: a nationwide study.
|
28490599 |
2017 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
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
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
Calculating the optimal surveillance for head and neck paraganglioma in SDHB-mutation carriers.
|
27573198 |
2017 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations.
|
28374168 |
2017 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
GeneticVariation |
CLINVAR |
The phenotype of SDHB germline mutation carriers: a nationwide study.
|
28490599 |
2017 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
A Duodenal SDH-Deficient Gastrointestinal Stromal Tumor in a Patient With a Germline SDHB Mutation.
|
28324028 |
2017 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
GeneticVariation |
CLINVAR |
SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations.
|
28374168 |
2017 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
A SDHC Founder Mutation Causes Paragangliomas (PGLs) in the French Canadians: New Insights on the SDHC-Related PGL.
|
27700540 |
2016 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
Attention Deficit Hyperactivity Disorder in Pediatric Patients with Pheochromocytoma and Paraganglioma.
|
27171833 |
2016 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
Magnetic resonance imaging spectrum of succinate dehydrogenase-related infantile leukoencephalopathy.
|
26642834 |
2016 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
GeneticVariation |
CLINVAR |
Novel SDHB and TMEM127 Mutations in Patients with Pheochromocytoma/Paraganglioma Syndrome.
|
26960314 |
2016 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster Delivery.
|
26719882 |
2016 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
Rapid-sequence MRI for long-term surveillance for paraganglioma and phaeochromocytoma in patients with succinate dehydrogenase mutations.
|
27634942 |
2016 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
Mediastinal paragangliomas related to SDHx gene mutations.
|
27785149 |
2016 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
GeneticVariation |
CLINVAR |
Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients.
|
27279923 |
2016 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
Sporadic paraganglioma caused by de novo SDHB mutations in a 6-year-old girl.
|
26283294 |
2016 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
Carney triad can be (rarely) associated with germline succinate dehydrogenase defects.
|
26173966 |
2016 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
GeneticVariation |
CLINVAR |
Association of urinary bladder paragangliomas with germline mutations in the SDHB and VHL genes.
|
25683602 |
2015 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
Toward an improved definition of the genetic and tumor spectrum associated with SDH germ-line mutations.
|
25394176 |
2015 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
Structural and functional consequences of succinate dehydrogenase subunit B mutations.
|
25972245 |
2015 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
CausalMutation |
CLINVAR |
15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5.
|
26273102 |
2015 |
Entrez Id: |
6390 |
Gene Symbol: |
SDHB |
SDHB
|
Neoplastic Syndromes, Hereditary
|
0.110 |
GeneticVariation |
CLINVAR |
Structural and functional consequences of succinate dehydrogenase subunit B mutations.
|
25972245 |
2015 |