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Genetics of Pheochromocytomas and Paragangliomas Determine the Therapeutical Approach

Genetics of Pheochromocytomas and Paragangliomas Determine the Therapeutical Approach

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8836037

Genetics of Pheochromocytomas and Paragangliomas Determine the Therapeutical Approach

About this item

Full title

Genetics of Pheochromocytomas and Paragangliomas Determine the Therapeutical Approach

Publisher

Switzerland: MDPI AG

Journal title

International journal of molecular sciences, 2022-01, Vol.23 (3), p.1450

Language

English

Formats

Publication information

Publisher

Switzerland: MDPI AG

More information

Scope and Contents

Contents

Pheochromocytomas and paragangliomas are the most heritable endocrine tumors. In addition to the inherited mutation other driver mutations have also been identified in tumor tissues. All these genetic alterations are clustered in distinct groups which determine the pathomechanisms. Most of these tumors are benign and their surgical removal will res...

Alternative Titles

Full title

Genetics of Pheochromocytomas and Paragangliomas Determine the Therapeutical Approach

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8836037

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8836037

Other Identifiers

ISSN

1422-0067,1661-6596

E-ISSN

1422-0067

DOI

10.3390/ijms23031450

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