Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder

BACKGROUND: Autism spectrum disorder (ASD) is an early-onset neurodevelopmental disorder with complex genetic underpinning in its etiology. Copy number variations (CNVs) as one of the genetic factors associated with ASD have been addressed in recent genome-wide association studies (GWAS). However, t...

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Detalles Bibliográficos
Autores principales: Yin, Chia-Lin, Chen, Hsin-I, Li, Ling-Hui, Chien, Yi-Ling, Liao, Hsiao-Mei, Chou, Miao Chun, Chou, Wen-Jiun, Tsai, Wen-Che, Chiu, Yen-Nan, Wu, Yu-Yu, Lo, Chen-Zen, Wu, Jer-Yuarn, Chen, Yuan-Tsong, Gau, Susan Shur-Fen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818409/
https://www.ncbi.nlm.nih.gov/pubmed/27042285
http://dx.doi.org/10.1186/s13229-016-0087-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818409/
https://www.ncbi.nlm.nih.gov/pubmed/27042285
http://dx.doi.org/10.1186/s13229-016-0087-7

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