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Phenotype and imaging features associated with APP duplications

Phenotype and imaging features associated with APP duplications

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_88847a664cd34093ae31f3d54233ce99

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

APP duplication is a rare genetic cause of Alzheimer disease and cerebral amyloid angiopathy (CAA). We aimed to evaluate the phenotypes of APP duplications carriers.
Clinical, radiological, and neuropathological features of 43 APP duplication carriers from 24 French families were retrospectively analyzed, and MRI features and cerebrospinal fluid...

Alternative Titles

Full title

Phenotype and imaging features associated with APP duplications

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_88847a664cd34093ae31f3d54233ce99

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_88847a664cd34093ae31f3d54233ce99

Other Identifiers

ISSN

1758-9193

E-ISSN

1758-9193

DOI

10.1186/s13195-023-01172-2

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