Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation-Reference-Cited by-同舟云学术

Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation

Published:2013-06-03 Issue:3 Volume:10 Page:360-365
ISSN:1552-5260
Container-title:Alzheimer's & Dementia
language:en
Short-container-title:Alzheimer's & Dementia

Author:

Carney Regina M.¹,Kohli Martin A.¹,Kunkle Brian W.¹,Naj Adam C.¹,Gilbert John R.¹²,Züchner Stephan¹²,Pericak‐Vance Margaret A.¹²

Affiliation:

1. University of Miam, Miller School of MedicineJohn P. Hussman Institute for Human GenomicsMiamiFLUSA

2. University of Miami, Miller School of MedicineDr. John T. Macdonald Foundation Department of Human GeneticsMiamiFLUSA

Funder

Alzheimer's Association

American Health Assistance Foundation

U.S. Department of Defense

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1016/j.jalz.2013.02.011

Reference40 articles.

1. What is ‘early onset dementia’?

2. Diagnosis of Alzheimer's Disease

3. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

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

5. Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

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