Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/125888
Title: Distinct X-chromosome SNVs from some sporadic AD samples
Author: Gómez-Ramos, A.
Podlesniy, P.
Soriano García, Eduardo
Avila, Jesús
Keywords: Malaltia d'Alzheimer
Nucleòtids
Alzheimer's disease
Nucleotides
Issue Date: 9-Dec-2015
Publisher: Nature Publishing Group
Abstract: Sporadic Alzheimer disease (SAD) is the most prevalent neurodegenerative disorder. With the development of new generation DNA sequencing technologies, additional genetic risk factors have been described. Here we used various methods to process DNA sequencing data in order to gain further insight into this important disease. We have sequenced the exomes of brain samples from SAD patients and non-demented controls. Using either method, we found a higher number of single nucleotide variants (SNVs), from SAD patients, in genes present at the X chromosome. Using the most stringent method, we validated these variants by Sanger sequencing. Two of these gene variants, were found in loci related to the ubiquitin pathway (UBE2NL and ATXN3L), previously do not described as genetic risk factors for SAD.
Note: Reproducció del document publicat a: https://doi.org/10.1038/srep18012
It is part of: Scientific Reports, 2015, vol. 5, p. 18012
URI: http://hdl.handle.net/2445/125888
Related resource: https://doi.org/10.1038/srep18012
ISSN: 2045-2322
Appears in Collections:Articles publicats en revistes (Biologia Cel·lular, Fisiologia i Immunologia)

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