Single base substitution mutational signatures in pediatric acute myeloid leukemia based on whole genome sequencing
Leukemia
.
2021 May;35(5):1485-1489.
doi: 10.1038/s41375-021-01242-0.
Epub 2021 Apr 16.
Authors
Rebeqa Gunnarsson
#
1
,
Minjun Yang
#
2
,
Linda Olsson-Arvidsson
2
3
,
Andrea Biloglav
2
,
Mikael Behrendtz
4
,
Anders Castor
5
,
Kajsa Paulsson
2
,
Bertil Johansson
2
3
Affiliations
1
Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden. rebeqa.gunnarsson@med.lu.se.
2
Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
3
Department of Clinical Genetics and Pathology, Division of Laboratory Medicine, Lund, Sweden.
4
Department of Pediatrics, Linköping University Hospital, Linköping, Sweden.
5
Department of Pediatrics, Skåne University Hospital, Lund, Sweden.
#
Contributed equally.
PMID:
33864028
PMCID:
PMC8102186
DOI:
10.1038/s41375-021-01242-0
No abstract available
Publication types
Letter
Research Support, Non-U.S. Gov't
MeSH terms
DNA Mutational Analysis / methods
Genome, Human / genetics*
Humans
Leukemia, Myeloid, Acute / genetics*
Mutation / genetics*
Whole Genome Sequencing / methods