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Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma

Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4282994

Publication information

Publisher

New York: Nature Publishing Group US

More information

Scope and Contents

Contents

Nada Jabado and colleagues report identification of gain-of-function mutations in
ACVR1
, which encodes activin A receptor type I, in midline pediatric high-grade astrocytomas.
Pediatric midline high-grade astrocytomas (mHGAs) are incurable with few treatment targets identified. Most tumors harbor mutations encoding p.Lys27Met in histone H...

Alternative Titles

Full title

Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4282994

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4282994

Other Identifiers

ISSN

1061-4036

E-ISSN

1546-1718

DOI

10.1038/ng.2950

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