Abstract: Abstract Neurofibromatosis type I (NF1) is a common, autosomal dominant condition that manifests as multiple café‐au‐lait spots, peripheral nerve sheath tumors, optic nerve pathway tumors, orthopedic abnormalities and learning disabilities. The gene for NF1 encodes neurofibromin, a large protein that downregulates intracellular Ras signaling.
Publication Year: 2006
Publication Date: 2006-01-27
Language: en
Type: other
Indexed In: ['crossref']
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Cited By Count: 2
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