MeSH(Medical Subject Headings) 맞춤 검색 (http://www.nlm.nih.gov) 결과 : 1 페이지: 1
Neurofibromin 1 - 새창
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.
Synonyms : NF-1 Protein, NF1 GRP, NF1 Protein, NF1-GAP-Related Protein, Neurofibromatosis Type 1 Gene Product, Neurofibromin, NF 1 Protein, NF1 GAP Related Protein
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MeSH(Medical Subject Headings) 유사 검색 (http://www.nlm.nih.gov) 결과 : 0 페이지: 1
