Cargando…
An insight into the understanding of 5-HTR2A variants leading to schizophrenia
Autores principales: | Lingaiah, Kusuma, Ramachandra, Nallur B. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4365344/ https://www.ncbi.nlm.nih.gov/pubmed/25758569 |
Ejemplares similares
-
Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: A copy number variation approach
por: Suresh, Raviraj V., et al.
Publicado: (2017) -
An understanding of spinocerebellar ataxia
por: Ramachandra, N.B., et al.
Publicado: (2015) -
A rare case of congenital heart disease with ambiguous genitalia
por: Lingaiah, Kusuma, et al.
Publicado: (2010) -
Mutations of TFAP2B in congenital heart disease patients in Mysore, South India
por: Lingaiah, Kusuma, et al.
Publicado: (2011) -
Evaluation of association of common variants in HTR1A and HTR5A with schizophrenia and executive function
por: Guan, Fanglin, et al.
Publicado: (2016)