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Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease

Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389743/
https://www.ncbi.nlm.nih.gov/pubmed/30847376
http://dx.doi.org/10.1002/acn3.742
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spelling pubmed-63897432019-03-07 Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease Ann Clin Transl Neurol Corrigendum John Wiley and Sons Inc. 2019-02-25 /pmc/articles/PMC6389743/ /pubmed/30847376 http://dx.doi.org/10.1002/acn3.742 Text en © 2019 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Corrigendum
Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease
title Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease
title_full Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease
title_fullStr Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease
title_full_unstemmed Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease
title_short Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease
title_sort whole‐exome sequencing in 20,197 persons for rare variants in alzheimer's disease
topic Corrigendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389743/
https://www.ncbi.nlm.nih.gov/pubmed/30847376
http://dx.doi.org/10.1002/acn3.742