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Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain developm...

Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain developm...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10208970

Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development

About this item

Full title

Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development

Publisher

London: Nature Publishing Group UK

Journal title

Molecular psychiatry, 2023-04, Vol.28 (4), p.1647-1663

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Childhood apraxia of speech (CAS), the prototypic severe childhood speech disorder, is characterized by motor programming and planning deficits. Genetic factors make substantive contributions to CAS aetiology, with a monogenic pathogenic variant identified in a third of cases, implicating around 20 single genes to date. Here we aimed to identify mo...

Alternative Titles

Full title

Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10208970

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10208970

Other Identifiers

ISSN

1359-4184

E-ISSN

1476-5578

DOI

10.1038/s41380-022-01764-8

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