Associated Papers
Identification of a novel MYO1D variant associated with laterality defects, congenital heart diseases, and sperm defects in humans.
Yuan Z et al.
Frontiers of Medicine, 2024
Novel MYO1D Missense Variant Identified Through Whole Exome Sequencing and Computational Biology Analysis Expands the Spectrum of Causal Genes of Laterality Defects.
Alsafwani RS et al.
Frontiers in Medicine, 2021
Select a paper to view details