Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with d...
Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3
About this item
Full title
Author / Creator
Publisher
New York: Nature Publishing Group US
Journal title
Language
English
Formats
Publication information
Publisher
New York: Nature Publishing Group US
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Scope and Contents
Contents
Michael Zeschnigk and colleagues identify recurrent somatic mutations of
EIF1AX
and
SF3B1
in uveal melanomas with disomy 3. The
EIF1AX
mutations specifically alter the N-terminal tail of the protein and were found exclusively in tumors lacking
SF3B1
mutations.
Gene expression profiles and chromosome 3 copy number divide u...
Alternative Titles
Full title
Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4307600
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4307600
Other Identifiers
ISSN
1061-4036
E-ISSN
1546-1718
DOI
10.1038/ng.2674
