Recent Advancement of Neurofibromatosis Type 1: A Narrative Review
Neurofibromatosis type 1 (NF1) is a complex autosomal dominant genetic disorder caused by mutations in the NF1 gene on chromosome 17, which encodes the tumor-suppressor protein, neurofibromin. Neurofibromin plays a critical role in regulating the RAS signaling pathway, and its loss leads to uncontro...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2025-04-01
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| Series: | Acta Neurologica Taiwanica |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/ant.ANT-D-24-00042 |
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