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

• Prif Awduron: Andrea Bieder (Awdur), Elisabet Einarsdottir (Awdur), Hans Matsson (Awdur), Harriet E. Nilsson (Awdur), Jesper Eisfeldt (Awdur), Anca Dragomir (Awdur), Martin Paucar (Awdur), Tobias Granberg (Awdur), Tie-Qiang Li (Awdur), Anna Lindstrand (Awdur), Juha Kere (Awdur), Isabel Tapia-Páez (Awdur)
• Fformat: Llyfr
• Cyhoeddwyd: BMC, 2020-05-01T00:00:00Z.
• Pynciau: article
• Mynediad Ar-lein: Connect to this object online.

Abstract 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 e...