RAS and beyond: the many faces of the neurofibromatosis type 1 protein
Neurofibromatosis type 1 is a rare neurogenetic syndrome, characterized by pigmentary abnormalities, learning and social deficits, and a predisposition for benign and malignant tumor formation caused by germline mutations in the NF1 gene. With the cloning of the NF1 gene and the recognition that the...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
The Company of Biologists
2022-02-01
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| Edice: | Disease Models & Mechanisms |
| Témata: | |
| On-line přístup: | http://dmm.biologists.org/content/15/2/dmm049362 |
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