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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4332023/
https://www.ncbi.nlm.nih.gov/pubmed/25694803
http://dx.doi.org/10.1186/2040-2392-5-44

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4332023/
https://www.ncbi.nlm.nih.gov/pubmed/25694803
http://dx.doi.org/10.1186/2040-2392-5-44

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