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Secondary association of PDLIM5 with paranoid schizophrenia in Emirati patients.
Moselhy, Hamdy; Eapen, Valsamma; Akawi, Nadia A; Younis, Ali; Salih, Badr; Othman, Aws R; Yousef, Said; Clarke, Raymond A; Ali, Bassam R.
Afiliação
  • Moselhy H; Department of Psychiatry, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.
  • Eapen V; University of New South Wales, Australia; Ingham Institute, School of Medicine, University of Western Sydney, Sydney, NSW, Australia.
  • Akawi NA; Department of Pathology, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.
  • Younis A; Al-Ain Hospital, Al-Ain, United Arab Emirates.
  • Salih B; Al-Ain Hospital, Al-Ain, United Arab Emirates.
  • Othman AR; Department of Pathology, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.
  • Yousef S; Department of Psychiatry, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.
  • Clarke RA; Ingham Institute, School of Medicine, University of Western Sydney, Sydney, NSW, Australia.
  • Ali BR; Department of Pathology, College of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.
Meta Gene ; 5: 135-9, 2015 Sep.
Article em En | MEDLINE | ID: mdl-26925374
Schizophrenia is a clinically and genetically heterogeneous disorder of unknown etiology. PDLIM5 variants have been linked to schizophrenia and other related neuropsychiatric disorders and upregulated in the brain of schizophrenia patients suggesting a possible pathogenic role in disease progression. The aim of this study is to examine the potential association of schizophrenia in Emirati patients with previously reported variants in PDLIM5, PICK1, NRG3 or DISC1 genes. Consequently, we found a secondary association between PDLIM5 variants and the paranoid subtype of schizophrenia in Emirati Arabs suggesting that PDLIM5 may represent a determinate/marker for schizophrenia subtype specification. However, no associations were found with variants in PICK1, NRG3 or DISC1 genes.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2015 Tipo de documento: Article