(Q36121934)

12 August 2017

1 reference

title

SDHC mutations in hereditary paraganglioma/pheochromocytoma (English)

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12 August 2017

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Ulrich Müller

1

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PubMed ID

15883704

12 August 2017

Christian Troidl

series ordinal

2

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PubMed ID

15883704

12 August 2017

Stephan Niemann

series ordinal

3

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12 August 2017

1 January 2005

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12 August 2017

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12 August 2017

4

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12 August 2017

1

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12 August 2017

9-12

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https://scigraph.springernature.com/pub.10.1007/s10689-004-0621-1

12 August 2017

0 references

cites work

Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma

1 reference

12 December 2020

The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway

1 reference

12 December 2020

Repositioning the hereditary paraganglioma critical region on chromosome band 11q23.

1 reference

12 December 2020

Genomic imprinting in hereditary glomus tumours: evidence for new genetic theory

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

1 reference

12 December 2020

Molecular genetics of succinate:quinone oxidoreductase in eukaryotes.

1 reference

12 December 2020

Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.

1 reference

12 December 2020

Oxidative phosphorylation at the fin de siècle

1 reference

12 December 2020

Familial carotid body tumors: case report and epidemiologic review

1 reference

12 December 2020

An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma

1 reference

12 December 2020

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter

1 reference

12 December 2020

Hereditary paraganglioma targets diverse paraganglia

1 reference

12 December 2020

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

1 reference

12 December 2020

Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC.

1 reference

12 December 2020

Germ-line mutations in nonsyndromic pheochromocytoma

1 reference

12 December 2020

PGL3, a third, not maternally imprinted locus in autosomal dominant paraganglioma

1 reference

12 December 2020

Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity

1 reference

12 December 2020

10.1007/S10689-004-0621-1

Identifiers

DOI

1 reference

12 August 2017

1 reference

PubMed ID

15883704