Associated Papers
Dynamics and recognition of homeodomain containing protein-DNA complex of IRX4.
Malik A et al.
Proteins, 2024
Human Genetics of Ventricular Septal Defect.
Perrot A et al.
Advances in Experimental Medicine and Biology, 2024
An update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations.
Li YJ et al.
Expert Review of Molecular Diagnostics, 2017
28274167 (PubMed )
Supplement: supplement_1.doc
Two novel mutations of the IRX4 gene in patients with congenital heart disease.
Cheng Z et al.
Human Genetics, 2011
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