A significant risk locus on 19q13 for bipolar disorder identified using a combined genome-wide linkage and copy number variation analysis

BACKGROUND: The genetic background to bipolar disorder (BPD) has been attributed to different genetic and genomic risk factors. In the present study we hypothesized that inherited copy number variations (CNVs) contribute to susceptibility of BPD. We screened 637 BP-pedigrees from the NIMH Genetic In...

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Detalles Bibliográficos
Autores principales: Lekman, Magnus, Karlsson, Robert, Graae, Lisette, Hössjer, Ola, Kockum, Ingrid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683747/
https://www.ncbi.nlm.nih.gov/pubmed/26692414
http://dx.doi.org/10.1186/s13040-015-0076-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683747/
https://www.ncbi.nlm.nih.gov/pubmed/26692414
http://dx.doi.org/10.1186/s13040-015-0076-y

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