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Assessment of somatic single-nucleotide variation in brain tissue of cases with schizophrenia
The genetic architecture of schizophrenia (SCZ) includes numerous risk loci across a range of frequencies and sizes, including common and rare single-nucleotide variants and insertions/deletions (indels), as well as rare copy number variants (CNVs). Despite the clear heritability of the disease, mon...
Autores principales: | Fullard, John F., Charney, Alexander W., Voloudakis, Georgios, Uzilov, Andrew V., Haroutunian, Vahram, Roussos, Panos |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336839/ https://www.ncbi.nlm.nih.gov/pubmed/30655504 http://dx.doi.org/10.1038/s41398-018-0342-0 |
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