High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan

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...

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Gepubliceerd in:Sci Rep
Hoofdauteurs: Chen, Chia-Hsiang, Chen, Hsin-I., Chien, Wei-Hsien, Li, Ling-Hui, Wu, Yu-Yu, Chiu, Yen-Nan, Tsai, Wen-Che, Gau, Susan Shur-Fen
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Nature Publishing Group UK 2017
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Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5607249/
https://ncbi.nlm.nih.gov/pubmed/28931914
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-12081-4
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