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Grant Award View - GA201625
Discovery of novel inborn errors of immunity that underlie Common...
GA ID:
GA201625
Agency:
National Health and Medical Research Council (NHMRC)
Approval Date:
19-Aug-2021
Publish Date:
10-Nov-2021
Category:
Medical Research
Grant Term:
1-Jan-2022 to 31-Dec-2026
Value (AUD):
$715,814.00
(GST inclusive where applicable)
One-off/Ad hoc:
No
Aggregate Grant Award:
No
PBS Program Name:
NHMRC 20/21 1.1 Health and Medical Research
Grant Program:
Investigator Grants
Grant Activity:
Discovery of novel inborn errors of immunity that underlie Common Variable Immunodeficiency
Purpose:
My research will study the underlying causes of Common Variable Immunodeficiency (CVID), the most common type of inherited immunodeficiency. It is caused by mutations in genes that are important for normal immune function. However, diagnosis is complex as many different gene mutations cause CVID, and most are still unknown. This research will identify new gene mutations and determine how they cause disease. The findings will support future gene-based diagnoses and guide targeted therapies.
GO ID:
GO Title:
Investigator Grants 2021
Internal Reference ID:
2021/GNT2007884
Selection Process:
Targeted or Restricted Competitive
Confidentiality - Contract:
Yes
Confidentiality Reason(s) - Contract:
Privacy Act 1988
Intellectual property
Intellectual property
Confidentiality - Outputs:
Yes
Confidentiality Reason(s) - Outputs:
Intellectual property
Grant Recipient Details
Recipient Name:
The Walter and Eliza Hall Institute of Medical Research
Recipient ABN:
12 004 251 423
Grant Recipient Location
Suburb:
Parkville
Town/City:
Parkville
Postcode:
3052
State/Territory:
VIC
Country:
AUSTRALIA
Grant Delivery Location
State/Territory:
VIC
Postcode:
Country:
AUSTRALIA