A particular GAP in mind

Y. Zhu, L. R. Parada

Research output: Contribution to journalShort survey

10 Scopus citations

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 languageEnglish (US)
Pages (from-to)354-355
Number of pages2
JournalNature genetics
Volume27
Issue number4
DOIs
StatePublished - Apr 17 2001

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ASJC Scopus subject areas

  • Genetics

Cite this

Zhu, Y., & Parada, L. R. (2001). A particular GAP in mind. Nature genetics, 27(4), 354-355. https://doi.org/10.1038/86835