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Grant Award View - GA29863
Deciphering the pathogenetics of rare diseases by multi-omic approaches:...
GA ID:
GA29863
Agency:
National Health and Medical Research Council (NHMRC)
Approval Date:
25-Oct-2018
Publish Date:
21-Dec-2018
Category:
Medical Research
Grant Term:
1-Jan-2019 to 31-Dec-2021
Value (AUD):
$1,145,702.97
(GST inclusive where applicable)
One-off/Ad hoc:
No
Aggregate Grant Award:
No
PBS Program Name:
NHMRC 17/18 1.1 Health and Medical Research
Grant Program:
Project
Grant Activity:
Deciphering the pathogenetics of rare diseases by multi-omic approaches: disorders of mitochondrial energy generation as an exemplar
Purpose:
More than 7000 inherited rare diseases are known. Although individually rare, these disorders collectively affect at least 1 in 20 people and are estimated to account for about a quarter of admissions to children’s hospitals. Diagnosis was often impossible in the past but new genomic technologies now allow diagnosis of perhaps half of all such children. We seek to improve these approaches so that nearly 100 percent of children with inherited disorders of energy generation can be diagnosed.
GO ID:
GO Title:
NHMRC Project Grant Scheme
Internal Reference ID:
GNT1164479
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:
Murdoch Childrens Research Institute
Recipient ABN:
21 006 566 972
Grant Recipient Location
Suburb:
Parkville
Town/City:
Parkville
Postcode:
3052
State/Territory:
VIC
Country:
AUSTRALIA
Grant Delivery Location
State/Territory:
VIC, Overseas
Postcode:
Multiple
Country:
AUSTRALIA, UNITED STATES