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Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma

Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1549632304

Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma

About this item

Full title

Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma

Publisher

New York: Nature Publishing Group US

Journal title

Nature genetics, 2014-08, Vol.46 (8), p.877-880

Language

English

Formats

Publication information

Publisher

New York: Nature Publishing Group US

More information

Scope and Contents

Contents

Bin Tean Teh and colleagues report exome sequencing of 8 breast fibroadenomas and follow-up targeted sequencing in 90 additional samples. They find that 59% of samples contain somatic mutations in exon 2 of
MED12
, a mutational pattern shared with another female-specific benign tumor, uterine leiomyoma.
Fibroadenomas are the most common br...

Alternative Titles

Full title

Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1549632304

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1549632304

Other Identifiers

ISSN

1061-4036

E-ISSN

1546-1718

DOI

10.1038/ng.3037

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