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No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia
Recessive inheritance of gene disrupting alleles, either through homozygosity at a specific site or compound heterozygosity, have been demonstrated to underlie many Mendelian diseases and some complex psychiatric disorders. On the basis of exome sequencing data, an increased burden of complete knock...
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| I publikationen: | Eur J Hum Genet |
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| Huvudupphovsmän: | , , , , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Nature Publishing Group
2015
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4666583/ https://ncbi.nlm.nih.gov/pubmed/25370044 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2014.228 |
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