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ELMOD3‐SH2D6 gene fusion as a possible co‐star actor in autism spectrum disorder scenario
Autism spectrum disorder (ASD) is a group of neurodevelopmental disorders characterized by high heritability. It is known that genetic factors contribute to ASD pathogenesis. In particular, copy number variants (CNVs) are involved in ASD susceptibility and can affect gene expression regulation. 2p11...
Guardat en:
| Publicat a: | J Cell Mol Med |
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| Autors principals: | , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6991669/ https://ncbi.nlm.nih.gov/pubmed/31800155 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.14733 |
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