Projects funded by the NCN
Solving the puzzle of deep intronic splicing variants as missing elements in the genetic landscape of Usher syndrome
2020/37/N/NZ5/02800
Keywords:
deep intronic varaints Usher syndrome next generation sequencing genome sequencing RNA splicing minigene
Descriptors:
- NZ5_3: Pathogenesis of human diseases
- NZ5_5: Diagnostics in human diseases
Panel:
NZ5 - Human and animal noninfectious diseases: etiology, mechanisms, diagnosis and treatment of diseases, poisonings and injuries (without neurological diseases)
Host institution :
Instytut Fizjologii i Patologii Słuchu
woj. mazowieckie
Principal investigator (from the host institution):
Number of co-investigators in the project: 3
Call: PRELUDIUM 19 - announced on 2020-03-16
Amount awarded: 209 928 PLN
Project start date (Y-m-d): 2021-09-20
Project end date (Y-m-d): 2024-09-19
Project duration:: 36 months (the same as in the proposal)
Project status: Project completed
Project description
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