SDHC mutations in hereditary paraganglioma/pheochromocytoma (Q36121934)

12 August 2017

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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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12 August 2017

Christian Troidl

series ordinal

2

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12 August 2017

Stephan Niemann

series ordinal

3

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12 August 2017

publication date

1 January 2005

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volume

4

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issue

1

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page(s)

9-12

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

12 August 2017

exact match

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cites work

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

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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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

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12 December 2020

Molecular genetics of succinate:quinone oxidoreductase in eukaryotes.

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12 December 2020

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

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12 December 2020

Oxidative phosphorylation at the fin de siècle

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12 December 2020

Familial carotid body tumors: case report and epidemiologic review

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Hereditary paraganglioma targets diverse paraganglia

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Germ-line mutations in nonsyndromic pheochromocytoma

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12 December 2020

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

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12 December 2020

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

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12 December 2020

10.1007/S10689-004-0621-1

Identifiers

DOI

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12 August 2017

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