(Q47817141)

English

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

scientific article published in November 2000

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/11062460

Mutations in SDHC cause autosomal dominant paraganglioma, type 3. (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/11062460

1 reference

based on heuristic

inferred from title

author name string

Niemann S

1

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/11062460

Müller U

2

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/11062460

language of work or name

0 references

publication date

1 November 2000

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/11062460

Nature Genetics

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/11062460

26

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/11062460

3

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/11062460

268-270

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/11062460

https://scigraph.springernature.com/pub.10.1038/81551

0 references

Familial carotid body tumors: case report and epidemiologic review

1 reference

https://api.crossref.org/works/10.1038%2F81551

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F81551

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F81551

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F81551

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F81551

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F81551

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F81551

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytochrome b in human complex II (succinate-ubiquinone oxidoreductase): cDNA cloning of the components in liver mitochondria and chromosome assignment of the genes for the large (SDHC) and small (SDHD) subunits to 1q21 and 11q23

1 reference

https://api.crossref.org/works/10.1038%2F81551

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/11062460

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/11062460

ResearchGate publication ID

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