Associated Papers
Gene-Edited Human-Induced Pluripotent Stem Cell Lines to Elucidate DAND5 Function throughout Cardiac Differentiation.
Inácio JM et al.
Cells, 2023
A novel biallelic loss-of-function variant in DAND5 causes heterotaxy syndrome.
Ganapathi M et al.
Cold Spring Harbor Molecular Case Studies, 2022
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects.
Bolkier Y et al.
Journal of Medical Genetics, 2022
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