Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder

BACKGROUND: Retrotransposons have been implicated as causes of Mendelian disease, but their role in autism spectrum disorder (ASD) has not been systematically defined, because they are only called with adequate sensitivity from whole genome sequencing (WGS) data and a large enough cohort for this an...

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Detalles Bibliográficos
Autores principales: Borges-Monroy, Rebeca, Chu, Chong, Dias, Caroline, Choi, Jaejoon, Lee, Soohyun, Gao, Yue, Shin, Taehwan, Park, Peter J., Walsh, Christopher A., Lee, Eunjung Alice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8627061/
https://www.ncbi.nlm.nih.gov/pubmed/34838103
http://dx.doi.org/10.1186/s13100-021-00256-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8627061/
https://www.ncbi.nlm.nih.gov/pubmed/34838103
http://dx.doi.org/10.1186/s13100-021-00256-w

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