Abstract
Type 1 neurofibromatosis is a syndrome caused by mutation of the gene NF1, which encodes neurofibromin - a tumor suppressor related to the Ras GAP signaling proteins. A new study of mice that lack a splice variant of neurofibromin discloses learning impairments similar to those of people with neurofibromatosis, and raises questions about the signaling pathways implicating neurofibromin isoforms during synaptic plasticity.
Original language | English (US) |
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Pages (from-to) | 354-355 |
Number of pages | 2 |
Journal | Nature genetics |
Volume | 27 |
Issue number | 4 |
DOIs | |
State | Published - 2001 |
ASJC Scopus subject areas
- Genetics