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Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophrenia
Schizophrenia (SCZ) is a serious psychiatric disease with strong heritability. Its complexity is reflected by extensive genetic heterogeneity and much of the genetic liability remains unaccounted for. We applied a combined strategy involving detection of copy number variants (CNVs), whole-genome map...
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| Publicado no: | Sci Rep |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4829830/ https://ncbi.nlm.nih.gov/pubmed/27071546 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep24327 |
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