(Q43994098)

28 November 2017

title

Low prevalence of APP duplications in Swedish and Finnish patients with early-onset Alzheimer's disease (English)

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28 November 2017

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5

Hilkka Soininen

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28 November 2017

7

Martin Ingelsson

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28 November 2017

6

Lars Lannfelt

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28 November 2017

Elin S Blom

1

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28 November 2017

Jayashree Viswanathan

2

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28 November 2017

Lena Kilander

3

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28 November 2017

Seppo Helisalmi

4

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28 November 2017

Anna Glaser

8

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28 November 2017

Mikko Hiltunen

9

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28 November 2017

publication date

28 November 2007

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European Journal of Human Genetics

28 November 2017

published in

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28 November 2017

volume

16

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28 November 2017

issue

2

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28 November 2017

page(s)

171-175

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201966

28 November 2017

exact match

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cites work

The precursor of Alzheimer's disease amyloid A4 protein resembles a cell-surface receptor

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Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

21 January 2018

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Candidate gene for the chromosome 1 familial Alzheimer's disease locus

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201966

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201966

Reconstitution of gamma-secretase activity

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201966

Apolipoprotein E isoform-dependent amyloid deposition and neuritic degeneration in a mouse model of Alzheimer's disease

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201966

Presenile dementia and Alzheimer's disease in mongolism.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201966

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201966

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201966

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201966

A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid

21 January 2018

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The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Abeta protofibril formation

21 January 2018

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No evidence for tau duplications in frontal temporal dementia families showing genetic linkage to the tau locus in which tau mutations have not been found

21 January 2018

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N-myc regulates parkin expression

21 January 2018

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Mapping of the Down syndrome phenotype on chromosome 21 at the molecular level.

21 January 2018

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APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201966

Phenotype associated with APP duplication in five families

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201966

Molecular mapping of Alzheimer-type dementia in Down's syndrome.

21 January 2018

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Clinical and neuropsychological characteristics in familial and sporadic Alzheimer's disease: relation to apolipoprotein E polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201966

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.EJHG.5201966

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Dimensions Publication ID

28 November 2017

1017155525

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1 reference