High resolution analysis of rare copy number variants in patients with autism spectrum disorder from...
High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan
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Publisher
London: Nature Publishing Group UK
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Language
English
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Publisher
London: Nature Publishing Group UK
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Contents
Rare genomic copy number variations (CNVs) (frequency <1%) contribute a part to the genetic underpinnings of autism spectrum disorders (ASD). The study aimed to understand the scope of rare CNV in Taiwanese patients with ASD. We conducted a genome-wide CNV screening of 335 ASD patients (299 males, 36 females) from Taiwan using Affymetrix Genome-Wid...
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Full title
High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5607249
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5607249
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ISSN
2045-2322
E-ISSN
2045-2322
DOI
10.1038/s41598-017-12081-4
