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SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function an...

SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function an...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_939b1e803648458f978aa0c525329996

SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice

Publication information

Publisher

London: Nature Publishing Group UK

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Scope and Contents

Contents

SLITRK2 is a single-pass transmembrane protein expressed at postsynaptic neurons that regulates neurite outgrowth and excitatory synapse maintenance. In the present study, we report on rare variants (one nonsense and six missense variants) in
SLITRK2
on the X chromosome identified by exome sequencing in individuals with neurodevelopmental dis...

Alternative Titles

Full title

SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice

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Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_939b1e803648458f978aa0c525329996

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_939b1e803648458f978aa0c525329996

Other Identifiers

ISSN

2041-1723

E-ISSN

2041-1723

DOI

10.1038/s41467-022-31566-z

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