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

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 ci...

Source: BMC Medical Genetics - May 1, 2020 Category: Genetics & Stem Cells Authors: Andrea Bieder, Elisabet Einarsdottir, Hans Matsson, Harriet E. Nilsson, Jesper Eisfeldt, Anca Dragomir, Martin Paucar, Tobias Granberg, Tie-Qiang Li, Anna Lindstrand, Juha Kere and Isabel Tapia-P áez Tags: Case report Source Type: research