Identification of primary copy number variations reveal enrichment of Calcium, and MAPK pathways sensitizing secondary sites for autism
Abstract Background Autism is a neurodevelopmental condition with genetic heterogeneity. It is characterized by difficulties in reciprocal social interactions with strong repetitive behaviors and stereotyped interests. Copy number variations (CNVs) are genomic structural variations altering the geno...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
SpringerOpen
2020-12-01
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| Col·lecció: | Egyptian Journal of Medical Human Genetics |
| Matèries: | |
| Accés en línia: | https://doi.org/10.1186/s43042-020-00091-3 |
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