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Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans

Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_46989eed5d5545f397b38c9c2843f70f

Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Clonal hematopoiesis driven by somatic heterozygous
TET2
loss is linked to malignant degeneration via consequent aberrant DNA methylation, and possibly to cardiovascular disease via increased cytokine and chemokine expression as reported in mice. Here, we discover a germline
TET2
mutation in a lymphoma family. We observe neither unusual...

Alternative Titles

Full title

Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_46989eed5d5545f397b38c9c2843f70f

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_46989eed5d5545f397b38c9c2843f70f

Other Identifiers

ISSN

2041-1723

E-ISSN

2041-1723

DOI

10.1038/s41467-019-09198-7

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