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Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
Growing genetic evidence is converging in favor of common pathogenic mechanisms for autism spectrum disorders (ASD), intellectual disability (ID or mental retardation) and schizophrenia (SCZ), three neurodevelopmental disorders affecting cognition and behavior. Copy number variations and deleterious...
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| Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2011
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3204930/ https://ncbi.nlm.nih.gov/pubmed/21424692 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-011-0975-z |
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