Truncating mutations in APP cause a distinct neurological phenotype-Reference-Cited by-同舟云学术

Truncating mutations in APP cause a distinct neurological phenotype

Published:2016-08-04 Issue:3 Volume:80 Page:456-460
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Klein Steven¹,Goldman Alexander¹,Lee Hane²,Ghahremani Shahnaz³,Bhakta Viraj¹,Nelson Stanley F.¹²⁴,Martinez‐Agosto Julian A.¹²⁵^ORCID,

Affiliation:

1. Department of Human GeneticsDavid Geffen School of Medicine at University of CaliforniaLos Angeles, Los Angeles California

2. Department of Pathology and Laboratory MedicineDavid Geffen School of Medicine at University of CaliforniaLos Angeles, Los Angeles California

3. Department of Radiology

4. Division of Medical GeneticsDepartment of Pediatrics, David Geffen School of Medicine at University of CaliforniaLos Angeles, Los Angeles California

5. Jonsson Cancer CenterDavid Geffen School of Medicine at University of CaliforniaLos Angeles, Los Angeles California

Funder

March of Dimes Foundation

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.24727

Reference20 articles.

1. Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum

2. Three dimensions of the amyloid hypothesis: time, space and 'wingmen'

3. Behavioral and anatomical deficits in mice homozygous for a modified ?-amyloid precursor protein gene

4. An Overview of APP Processing Enzymes and Products

5. β-amyloid precursor protein-deficient mice show reactive gliosis and decreased locomotor activity

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