Cargando…
What can rare variant genetics tell us about cognition and intellectual difficulties?
Autores principales: | Thomas, Rhys H., Robertson, Neil P. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5110588/ https://www.ncbi.nlm.nih.gov/pubmed/27822598 http://dx.doi.org/10.1007/s00415-016-8326-6 |
Ejemplares similares
-
New rare genetic variants in multiple sclerosis
por: Harding, Katharine E., et al.
Publicado: (2018) -
The consequences of valproate exposure in utero
por: Thomas, Rhys H., et al.
Publicado: (2016) -
Cerebral amyloid angiopathy: subtypes, treatment and role in cognitive impairment
por: McLauchlan, D., et al.
Publicado: (2017) -
Advances in Tourette’s syndrome
por: Robertson, Neil P.
Publicado: (2023) -
Genetics of disease severity in multiple sclerosis, Alzheimer’s disease, and Huntington’s disease: rejuvenating genome-wide association studies
por: Hrastelj, James, et al.
Publicado: (2017)