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ARMC5 Mutations in Macronodular Adrenal Hyperplasia with Cushing's Syndrome

ARMC5 Mutations in Macronodular Adrenal Hyperplasia with Cushing's Syndrome

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4727443

ARMC5 Mutations in Macronodular Adrenal Hyperplasia with Cushing's Syndrome

About this item

Full title

ARMC5 Mutations in Macronodular Adrenal Hyperplasia with Cushing's Syndrome

Publisher

Waltham, MA: Massachusetts Medical Society

Journal title

The New England journal of medicine, 2013-11, Vol.369 (22), p.2105-2114

Language

English

Formats

Publication information

Publisher

Waltham, MA: Massachusetts Medical Society

More information

Scope and Contents

Contents

This study showed that there were mutations in
ARMC5,
a putative tumor-suppressor gene, in a substantial proportion of patients with corticotropin-independent macronodular adrenal hyperplasia, a finding that may be helpful in the diagnosis and management of this disease.
Corticotropin-independent macronodular adrenal hyperplasia can lead t...

Alternative Titles

Full title

ARMC5 Mutations in Macronodular Adrenal Hyperplasia with Cushing's Syndrome

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4727443

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4727443

Other Identifiers

ISSN

0028-4793

E-ISSN

1533-4406

DOI

10.1056/NEJMoa1304603