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Inherited human IFN-γ deficiency underlies mycobacterial disease

Inherited human IFN-γ deficiency underlies mycobacterial disease

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7260033

Inherited human IFN-γ deficiency underlies mycobacterial disease

Publication information

Publisher

United States: American Society for Clinical Investigation

More information

Scope and Contents

Contents

Mendelian susceptibility to mycobacterial disease (MSMD) is characterized by a selective predisposition to clinical disease caused by the Bacille Calmette-Guérin (BCG) vaccine and environmental mycobacteria. The known genetic etiologies of MSMD are inborn errors of IFN-γ immunity due to mutations of 15 genes controlling the production of or respons...

Alternative Titles

Full title

Inherited human IFN-γ deficiency underlies mycobacterial disease

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7260033

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7260033

Other Identifiers

ISSN

0021-9738,1558-8238

E-ISSN

1558-8238

DOI

10.1172/JCI135460

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