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Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood

Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b671baf57f4d42619acfe5843fbbb345

Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

TET3
encodes an essential dioxygenase involved in epigenetic regulation through DNA demethylation.
TET3
deficiency, or Beck-Fahrner syndrome (BEFAHRS; MIM: 618798), is a recently described neurodevelopmental disorder of the DNA demethylation machinery with a nonspecific phenotype resembling other chromatin-modifying disorders, but inconsis...

Alternative Titles

Full title

Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_b671baf57f4d42619acfe5843fbbb345

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b671baf57f4d42619acfe5843fbbb345

Other Identifiers

ISSN

2056-7944

E-ISSN

2056-7944

DOI

10.1038/s41525-021-00256-y

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