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Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia

Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6291354

Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia

About this item

Full title

Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia

Publisher

London: Nature Publishing Group UK

Journal title

Molecular psychiatry, 2020-04, Vol.25 (4), p.821-830

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Childhood-onset schizophrenia (COS) is a rare and severe form of schizophrenia defined as onset before age of 13. Here we report on two unrelated cases diagnosed with both COS and alternating hemiplegia of childhood (AHC), and for whom two distinct pathogenic de novo variants were identified in the
ATP1A3
gene.
ATP1A3
encodes the α-subu...

Alternative Titles

Full title

Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6291354

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6291354

Other Identifiers

ISSN

1359-4184,1476-5578

E-ISSN

1476-5578

DOI

10.1038/s41380-018-0103-8

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