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Identification of susceptibility gene mutations associated with the pathogenesis of familial nonmedu...

Identification of susceptibility gene mutations associated with the pathogenesis of familial nonmedu...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_f07c1d8baf304c8cbecaa6b13d421dd9

Identification of susceptibility gene mutations associated with the pathogenesis of familial nonmedullary thyroid cancer

About this item

Full title

Identification of susceptibility gene mutations associated with the pathogenesis of familial nonmedullary thyroid cancer

Publisher

United States: John Wiley & Sons, Inc

Journal title

Molecular genetics & genomic medicine, 2019-12, Vol.7 (12), p.e1015-n/a

Language

English

Formats

Publication information

Publisher

United States: John Wiley & Sons, Inc

More information

Scope and Contents

Contents

Background
Familial nonmedullary thyroid cancer (FNMTC) accounts for approximately 3%–9% of all thyroid cancers; however, the mechanisms underlying FNMTC remain unclear. Environmental and genetic (especially genetic mutation) factors may play important roles in FNMTC etiology, development, and pathogenesis.
Methods
Three affected members,...

Alternative Titles

Full title

Identification of susceptibility gene mutations associated with the pathogenesis of familial nonmedullary thyroid cancer

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_f07c1d8baf304c8cbecaa6b13d421dd9

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_f07c1d8baf304c8cbecaa6b13d421dd9

Other Identifiers

ISSN

2324-9269

E-ISSN

2324-9269

DOI

10.1002/mgg3.1015

How to access this item