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CRISPR-Cas9 to Cure Hereditary Anemia

CYSF · 2025

Liv Multani · Calgary Girls Charter School

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Overview

My project is about using CRISPR-Cas9 gene editing to cure hereditary aneimia, using my research and data points.

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Acknowledgement

I would like to acknowledge my teachers, and my school (CGCS) for supporting me to do this project. I would also like to acknowlage the following people for supporting, and helping out with my project: Harveer Khela, Jasmeen Khela, Rutvi Suryawnshi, Hamskia Chandramouli, Ritaj Al-Dulaimi, Suhavi Luthra, and Josie Daskal.

Awards (1)

  • HONOURABLE MENTION

Competition history

  • CYSF 2025 Category not listed

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Source: Calgary Youth Science Fair

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