(Q34186212)

English

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

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scholarly article

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Europe PubMed Central

PubMed publication ID

31 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1 reference

based on heuristic

inferred from title

author name string

Stephan Niemann

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Ulrich Müller

2

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Europe PubMed Central

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31 July 2017

Dieter Engelhardt

3

1 reference

Europe PubMed Central

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31 July 2017

Peter Lohse

4

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Europe PubMed Central

PubMed publication ID

31 July 2017

publication date

25 March 2003

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Europe PubMed Central

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31 July 2017

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Europe PubMed Central

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31 July 2017

113

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Europe PubMed Central

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31 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

92-94

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

https://scigraph.springernature.com/pub.10.1007/s00439-003-0938-0

0 references

Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/12658451

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nomenclature for the description of human sequence variations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12658451

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12658451

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12658451

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic dichotomy in mitochondrial complex II genetic disorders.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12658451

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The HUGO Gene Nomenclature Committee (HGNC).

1 reference

https://pubmed.ncbi.nlm.nih.gov/12658451

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary paraganglioma targets diverse paraganglia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12658451

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12658451

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12658451

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-003-0938-0

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Dimensions Publication ID

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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