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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:BMC Med Genet
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7193346/
https://ncbi.nlm.nih.gov/pubmed/32357925
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-01020-2
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados