학술논문

SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice.
Document Type
Article
Source
Nature Communications; 7/15/2022, Vol. 13 Issue 1, p1-19, 19p
Subject
X chromosome
NEURAL development
MEMBRANE proteins
BIOLOGICAL transport
PROTEIN-tyrosine kinases
GAIT disorders
Language
ISSN
20411723
Abstract
Copyright of Nature Communications is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)