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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...
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| Publicado no: | J Cell Mol Med |
|---|---|
| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2019
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| Assuntos: | |
| Acesso em linha: | 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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