Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia

BACKGROUND: Several copy number variants (CNVs) have been implicated as susceptibility factors for schizophrenia (SZ). Some of these same CNV also increase risk for autism spectrum disorders (ASD), suggesting an etiologic overlap between these conditions. Recently, de novo duplications of a region o...

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محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Mulle, Jennifer Gladys, Pulver, Ann E., McGrath, John M., Wolyniec, Paula, Dodd, Anne F., Cutler, David J., Sebat, Jonathan, Malhotra, Dheeraj, Nestadt, Gerald, Conrad, Donald F., Hurles, Matthew, Barnes, Chris P., Ikeda, Masashi, Iwata, Nakao, Levinson, Douglas F., Gejman, Pablo V., Sanders, Alan R., Duan, Jubao, Mitchell, Adele A., Peter, Inga, Sklar, Pamela, O’Dushlaine, Colm T., Grozeva, Detelina, O’Donovan, Michael C., Owen, Michael J., Hultman, Christina M., Kähler, Anna K., Sullivan, Patrick F., Kirov, George, Warren, Stephen T.
التنسيق: Artigo
اللغة:Inglês
منشور في: 2013
الموضوعات:
Article
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC3838485/
https://ncbi.nlm.nih.gov/pubmed/23871472
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biopsych.2013.05.040
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