(Q44347017)

English

Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas

scientific article published in March 2003

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scholarly article

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Europe PubMed Central

PubMed publication ID

2 December 2017

Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

10

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Bruce G Robinson

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Europe PubMed Central

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2 December 2017

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Diana E Benn

1

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Europe PubMed Central

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2 December 2017

Michael S Croxson

2

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Europe PubMed Central

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2 December 2017

Kathy Tucker

3

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Europe PubMed Central

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2 December 2017

Christopher P Bambach

4

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Europe PubMed Central

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2 December 2017

Anne Louise Richardson

5

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Europe PubMed Central

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2 December 2017

Leigh Delbridge

6

1 reference

Europe PubMed Central

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2 December 2017

Peter T Pullan

7

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Europe PubMed Central

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2 December 2017

Jeremy Hammond

8

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2 December 2017

Deborah J Marsh

9

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2 December 2017

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publication date

1 March 2003

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2 December 2017

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2 December 2017

22

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2 December 2017

9

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Europe PubMed Central

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2 December 2017

1358-1364

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Europe PubMed Central

PubMed publication ID

2 December 2017

Germline SDHD mutation in familial phaeochromocytoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetics of familial paragangliomas: past, present, and future

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

based on heuristic

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Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

based on heuristic

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Phenotypic dichotomy in mitochondrial complex II genetic disorders.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

based on heuristic

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Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas

1 reference

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7 January 2021

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Chromosome bands 1p35-36 contain two distinct neuroblastoma tumor suppressor loci, one of which is imprinted

1 reference

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7 January 2021

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Loss of Heterozygosity on the Short Arm of Chromosome 1 in Pheochromocytoma and Abdominal Paraganglioma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

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Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

based on heuristic

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Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

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Somatic VHL gene deletion and point mutation in MEN 2A-associated pheochromocytoma

1 reference

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7 January 2021

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All in the (cancer) family

1 reference

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Familial abdominal chemodectomas with associated cutaneous angiolipomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

based on heuristic

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The gene for the iron sulfur protein of succinate dehydrogenase (SDH-IP) maps to human chromosome 1p35-36.1.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

based on heuristic

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Germ-line mutations in nonsyndromic pheochromocytoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular genetics of succinate:quinone oxidoreductase in eukaryotes.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

based on heuristic

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A second leaky splice-site mutation in the spastin gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

based on heuristic

inferred from DOI database lookup

Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

based on heuristic

inferred from DOI database lookup

Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1206300

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.ONC.1206300

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

ResearchGate publication ID

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