Rare variants and handedness: spotlight on TUBB4B.
Trends Genet
; 40(7): 558-559, 2024 Jul.
Article
en En
| MEDLINE
| ID: mdl-38749881
ABSTRACT
Twin studies suggest that additive genetic effects account for about a quarter of the variance in handedness. Recently, Schijven et al. used exome-wide sequencing to provide evidence for a role of rare protein-coding variants in handedness. These included the gene encoding beta-tubulin, TUBB4B, suggesting that microtubules are relevant for handedness ontogenesis.
Palabras clave
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Tubulina (Proteína)
/
Lateralidad Funcional
Límite:
Humans
Idioma:
En
Revista:
Trends Genet
Asunto de la revista:
GENETICA
Año:
2024
Tipo del documento:
Article
Pais de publicación:
Reino Unido