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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607249/
https://www.ncbi.nlm.nih.gov/pubmed/28931914
http://dx.doi.org/10.1038/s41598-017-12081-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607249/
https://www.ncbi.nlm.nih.gov/pubmed/28931914
http://dx.doi.org/10.1038/s41598-017-12081-4

Ejemplares similares