Molecular Basis of Fracture Pseudarthrosis Associated with Neurofibromatosis Type 1
Neurofibromatosis Type 1 (NF1) is a tumor-predisposition syndrome caused by heterozygous mutations in the NF1 gene. In addition to oncologic manifestations, individuals with NF1 face a heightened risk of developing secondary skeletal complications associated with somatic loss-of-heterozygosity. Long...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2025-08-01
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| Series: | Journal of the Pediatric Orthopaedic Society of North America |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S276827652500046X |
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