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Whole Exome-Wide Association Identifies Rare Variants in IGALNT9/I Associated with Middle Eastern Pa...

Whole Exome-Wide Association Identifies Rare Variants in IGALNT9/I Associated with Middle Eastern Pa...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A764264587

Whole Exome-Wide Association Identifies Rare Variants in IGALNT9/I Associated with Middle Eastern Papillary Thyroid Carcinoma Risk

About this item

Full title

Whole Exome-Wide Association Identifies Rare Variants in IGALNT9/I Associated with Middle Eastern Papillary Thyroid Carcinoma Risk

Publisher

MDPI AG

Journal title

Cancers, 2023-08, Vol.15 (17)

Language

English

Formats

Publication information

Publisher

MDPI AG

More information

Scope and Contents

Contents

This study targeted the identification of rare variants in Middle Eastern papillary thyroid carcinoma (PTC) through an exome-wide association study. It was found that the GALNT9 gene was strongly associated with rare inactivating variants. Three genes (TRIM40, ARHGAP23, and SOX4) were associated with rare damaging variants (RDVs). Furthermore, seve...

Alternative Titles

Full title

Whole Exome-Wide Association Identifies Rare Variants in IGALNT9/I Associated with Middle Eastern Papillary Thyroid Carcinoma Risk

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_gale_infotracmisc_A764264587

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A764264587

Other Identifiers

ISSN

2072-6694

E-ISSN

2072-6694

DOI

10.3390/cancers15174235

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