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Rare variants and handedness: spotlight on TUBB4B.
Ocklenburg, Sebastian.
Afiliación
  • Ocklenburg S; Department of Psychology, MSH Medical School Hamburg, Hamburg, Germany; ICAN Institute for Cognitive and Affective Neuroscience, MSH Medical School Hamburg, Hamburg, Germany; Biopsychology, Institute of Cognitive Neuroscience, Faculty of Psychology, Ruhr University Bochum, Bochum, Germany. Electronic address: sebastian.ocklenburg@medicalschool-hamburg.de.
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.
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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

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