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Solving for X: evidence for sex-specific autism biomarkers across multiple transcriptomic studies
Autism spectrum disorder (ASD) is a markedly heterogeneous condition with a varied phenotypic presentation. Its high concordance among siblings, as well as its clear association with specific genetic disorders, both point to a strong genetic etiology. However, the molecular basis of ASD is still poo...
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| Publicat a: | Am J Med Genet B Neuropsychiatr Genet |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6551334/ https://ncbi.nlm.nih.gov/pubmed/30520558 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.32701 |
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