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Structural brain anomalies in patients with FOXG 1 syndrome and in Foxg1+/− mice

Structural brain anomalies in patients with FOXG 1 syndrome and in Foxg1+/− mice

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2244271639

Structural brain anomalies in patients with FOXG 1 syndrome and in Foxg1+/− mice

Publication information

Publisher

Bognor Regis: John Wiley & Sons, Inc

More information

Scope and Contents

Contents

ObjectiveFOXG1 syndrome is a rare neurodevelopmental disorder associated with heterozygous FOXG1 variants or chromosomal microaberrations in 14q12. The study aimed at assessing the scope of structural cerebral anomalies revealed by neuroimaging to delineate the genotype and neuroimaging phenotype associations.MethodsWe compiled 34 patients with a h...

Alternative Titles

Full title

Structural brain anomalies in patients with FOXG 1 syndrome and in Foxg1+/− mice

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2244271639

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2244271639

Other Identifiers

ISSN

2328-9503

E-ISSN

2328-9503

DOI

10.1002/acn3.735

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