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

• Main Authors: Andrea Bieder (Author), Elisabet Einarsdottir (Author), Hans Matsson (Author), Harriet E. Nilsson (Author), Jesper Eisfeldt (Author), Anca Dragomir (Author), Martin Paucar (Author), Tobias Granberg (Author), Tie-Qiang Li (Author), Anna Lindstrand (Author), Juha Kere (Author), Isabel Tapia-Páez (Author)
• Format: Book
• Published: BMC, 2020-05-01T00:00:00Z.
• Subjects: article
• Online Access: 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...