proteín neurofibromatózy 1 proteín neurofibromatózy typu 1
English X references
Neurofibromatosis Type 1 Protein
Scope note in English
A protein found most abundantly in the nervous system. Defects or deficiencies in this protein are associated with NEUROFIBROMATOSIS 1, Watson syndrome, and LEOPARD syndrome. Mutations in the gene (GENE, NEUROFIBROMATOSIS 1) affect two known functions: regulation of ras-GTPase and tumor suppression.
See also reference (FX) in Slovak
gény neurofibromatózy 1 neurofibromatóza 1
See also reference (FX) in English
Genes, Neurofibromatosis 1 Neurofibromatosis 1
Links
(3) - ARTICLES
(2) - MeSH descriptor
subject heading
Number of the records: 1
openseadragon
This site uses cookies to make them easier to browse. Learn more about
how we use cookies.