Projects funded by the NCN
Dissecting the clinical complexity of 22q11 Deletion Syndrome by deep phenotyping and functional genomics.
2020/37/B/NZ5/03337
Keywords:
22q11 Deletion Syndrome phenotypic variation genome sequencing gene expression RNA-seq
Descriptors:
- NZ5_3: Pathogenesis of human diseases
- NZ2_2: Genomics, transcriptomics, epigenomics
Panel:
NZ5 - Human and animal noninfectious diseases: etiology, mechanisms, diagnosis and treatment of diseases, poisonings and injuries (without neurological diseases)
Host institution :
Instytut Matki i Dziecka
woj. mazowieckie
Principal investigator (from the host institution):
Number of co-investigators in the project: 3
Call: OPUS 19 - announced on 2020-03-16
Amount awarded: 1 940 520 PLN
Project start date (Y-m-d): 2021-02-22
Project end date (Y-m-d): 2024-02-21
Project duration:: 36 months (the same as in the proposal)
Project status: Project completed
Project description
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