Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report

BACKGROUND: Developmental dyslexia (DD) is a neurodevelopmental learning disorder with high heritability. A number of candidate susceptibility genes have been identified, some of which are linked to the function of the cilium, an organelle regulating left-right asymmetry development in the embryo. F...

Descripción completa

Detalles Bibliográficos
Autores principales: Bieder, Andrea, Einarsdottir, Elisabet, Matsson, Hans, Nilsson, Harriet E., Eisfeldt, Jesper, Dragomir, Anca, Paucar, Martin, Granberg, Tobias, Li, Tie-Qiang, Lindstrand, Anna, Kere, Juha, Tapia-Páez, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7193346/
https://www.ncbi.nlm.nih.gov/pubmed/32357925
http://dx.doi.org/10.1186/s12881-020-01020-2

Ejemplares similares

Ejemplares similares