Projects funded by the NCN
Searching for mutations in COL4A3, COL4A4 and COL4A5 genes and defining their impact on clinical outcome in a national cohort of Polish families with hematuria with the use of next-generation sequencing technology.
2017/25/N/NZ5/00466
Keywords:
Alport Syndrome thin basement membrane nephropathy familial hematuria collagen IV genetics Next-generation sequencing Polish patients
Descriptors:
- NZ5_1: Etiology of human diseases
- NZ2_1: Molecular genetics
Panel:
NZ5 - Human and animal noninfectious diseases: etiology, mechanisms, diagnosis and treatment of diseases, poisonings and injuries (without neurological diseases)
Host institution :
Gdański Uniwersytet Medyczny, Wydział Lekarski
woj. pomorskie
Principal investigator (from the host institution):
Number of co-investigators in the project: 3
Call: PRELUDIUM 13 - announced on 2017-03-15
Amount awarded: 180 000 PLN
Project start date (Y-m-d): 2018-03-28
Project end date (Y-m-d): 2022-03-27
Project duration:: 48 months (the same as in the proposal)
Project status: Project settled
Project description
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