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Article

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

BMC medical genetics - 1 May 2020

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

Abstract excerpt

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. Furthermore, it has been suggested that disrupted left-right asymmetry of the brain may play a role in...

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PMID: 32357925
DOI: 10.1186/s12881-020-01020-2
PMCID: PMC7193346

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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