Projects funded by the NCN
Determination of cytogeneic rearrangements:chromosomal aberrations and uniparental disomy in Barth Syndrome carriers to study the role of tafazzin in the mechanisms of inheritance of a genetic mosaicism
2016/21/N/NZ2/01729
Keywords:
genetic mosaicism tafazzin TAZ gene uniparental disomy chromosomal aberrations bart syndrome mechanisms of inheritance
Descriptors:
- NZ2_5: Cell genetics
- NZ2_1: Molecular genetics
- NZ1_1: Molecular biology
Panel:
NZ2 - Genetics, genomics: molecular genetics, genomics, proteomics, bioinformatics, systems biology, genetic epidemiology
Host institution :
Uniwersytet Jagielloński-Collegium Medicum, Collegium Medicum, Wydział Lekarski
woj. małopolskie
Principal investigator (from the host institution):
Number of co-investigators in the project: 3
Call: PRELUDIUM 11 - announced on 2016-03-15
Amount awarded: 150 000 PLN
Project start date (Y-m-d): 2017-02-27
Project end date (Y-m-d): 2022-02-26
Project duration:: 60 months (the same as in the proposal)
Project status: Project settled
Project description
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