Cargando…
Genome-Wide Supported Risk Variants in MIR137, CACNA1C, CSMD1, DRD2, and GRM3 Contribute to Schizophrenia Susceptibility in Pakistani Population
OBJECTIVE: Schizophrenia is a chronic neuropsychiatric disease afflicting around 1.1% of the population worldwide. Recently, MIR137, CACNA1C, CSMD1, DRD2, and GRM3 have been reported as the most robustly emerging candidates involved in the etiology of schizophrenia. In this case control study, we pe...
Autores principales: | Fatima, Ambrin, Farooq, Muhammad, Abdullah, Uzma, Tariq, Muhammad, Mustafa, Tanveer, Iqbal, Muhammad, Tommerup, Niels, Mahmood Baig, Shahid |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Neuropsychiatric Association
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5639139/ https://www.ncbi.nlm.nih.gov/pubmed/29042896 http://dx.doi.org/10.4306/pi.2017.14.5.687 |
Ejemplares similares
-
A Novel Nonsense Variant in GRM1 Causes Autosomal Recessive Spinocerebellar Ataxia 13 in a Consanguineous Pakistani Family
por: Yousaf, Hammad, et al.
Publicado: (2022) -
Rare Pathogenic Variants in Genes Implicated in Glutamatergic Neurotransmission Pathway Segregate with Schizophrenia in Pakistani Families
por: Fatima, Ambrin, et al.
Publicado: (2021) -
Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families
por: Zhou, Yingjie, et al.
Publicado: (2020) -
Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindness
por: Naeem, Muhammad Asif, et al.
Publicado: (2015) -
Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar Disorders
por: Saadi, Saadia Maryam, et al.
Publicado: (2023)