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  Rare autosomal copy number variations in early-onset familial Alzheimer's disease

Hooli, B. V., Kovacs-Vajna, Z. M., Mullin, K., Blumenthal, M. A., Mattheisen, M., Zhang, C., et al. (2014). Rare autosomal copy number variations in early-onset familial Alzheimer's disease. Molecular Psychiatry, 19(6), 676-681. doi:10.1038/mp.2013.77.

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mp201377a.pdf (Publisher version), 238KB
 
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2013-06-11
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 Creators:
Hooli, B V1, Author
Kovacs-Vajna, Z M2, Author
Mullin, K1, Author
Blumenthal, M A1, Author
Mattheisen, M 3, Author
Zhang, C1, Author
Lange, C4, Author
Mohapatra, G5, Author
Bertram, Lars6, Author           
Tanzi, R E1, Author
Affiliations:
1Department of Neurology, Genetics and Aging Research Unit, MassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital, , Charlestown, MA, USA, ou_persistent22              
2Department of Information Engineering, University of Brescia, Brescia, Italy, ou_persistent22              
3Channing Laboratory, Brigham and Women’s Hospital, Boston MA, USA, ou_persistent22              
4Department of Biostatistics, Harvard School of Public Health, Boston, MA, USA, ou_persistent22              
5Molecular Pathology Unit, Massachusetts General Hospital, Boston, MA, USA, ou_persistent22              
6Neuropsychiatric Genetics (Lars Bertram), Dept. of Vertebrate Genomics (Head: Hans Lehrach), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1479655              

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 Dates: 2013-03-192013-04-152013-06-112014-06-01
 Publication Status: Issued
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 Identifiers: DOI: 10.1038/mp.2013.77
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Funding program : This study was funded by grants from the NIMH and the Cure Alzheimer’s Fund.
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Title: Molecular Psychiatry
Source Genre: Journal
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Publ. Info: Houndmills, Hampshire, UK : Stockton Press
Pages: - Volume / Issue: 19 (6) Sequence Number: - Start / End Page: 676 - 681 Identifier: ISSN: 1359-4184
CoNE: https://pure.mpg.de/cone/journals/resource/954925619131