Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1

BACKGROUND: Duplications of the chromosome 15q11-q13.1 region are associated with an estimated 1 to 3% of all autism cases, making this copy number variation (CNV) one of the most frequent chromosome abnormalities associated with autism spectrum disorder (ASD). Several genes located within the 15q11...

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Detalhes bibliográficos
Publicado no:Mol Autism
Main Authors: Germain, Noelle D, Chen, Pin-Fang, Plocik, Alex M, Glatt-Deeley, Heather, Brown, Judith, Fink, James J, Bolduc, Kaitlyn A, Robinson, Tiwanna M, Levine, Eric S, Reiter, Lawrence T, Graveley, Brenton R, Lalande, Marc, Chamberlain, Stormy J
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4332023/
https://ncbi.nlm.nih.gov/pubmed/25694803
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2040-2392-5-44
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