Exhaustive non-synonymous variants functionality prediction enables high resolution characterization of the neurofibromin architectureResearch in context
Background: Neurofibromatosis type I (NF1) is caused by heterozygous loss-of-function variants in the NF1 gene encoding neurofibromin which serves as a tumor suppressor that inhibits RAS signaling and regulates cell proliferation and differentiation. While, the only well-established functional domai...
Gardado en:
| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Elsevier
2018-10-01
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| Series: | EBioMedicine |
| Acceso en liña: | http://www.sciencedirect.com/science/article/pii/S2352396418303979 |
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