Insights and future directions of potential genetic therapy for Apert syndrome: A systematic review
Apert syndrome is a genetic disorder characterised by craniosynostosis and structural discrepancy of the craniofacial region as well as the hands and feet. This condition is closely linked with fibroblast growth factor receptor-2 (FGFR2) gene mutations. Gene therapies are progressively being tested...
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| Main Authors: | , , , , |
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| Format: | Article |
| Published: |
Springernature
2021
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| Subjects: | |
| Online Access: | http://eprints.um.edu.my/27996/ |
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