Associated Papers
Identification of a De novo pathogenic missense variant (c.559G>A) in CASZ1 associated with dilated cardiomyopathy.
Liu RL et al.
Qjm : Monthly Journal of the Association of Physicians, 2024
Role of the CASZ1 transcription factor in tissue development and disease.
Liu T et al.
European Journal of Medical Research, 2023
Identification of a Novel de Novo Variant in the CASZ1 Causing a Rare Type of Dilated Cardiomyopathy.
Orlova A et al.
International Journal of Molecular Sciences, 2022
Overlap phenotypes of the left ventricular noncompaction and hypertrophic cardiomyopathy with complex arrhythmias and heart failure induced by the novel truncated DSC2 mutation.
Lin Y et al.
Orphanet Journal of Rare Diseases, 2021
Clinical Application of Whole Exome Sequencing for Monogenic Disorders in PICU of China.
Liu Y et al.
Frontiers in Genetics, 2021
A novel de novo CASZ1 heterozygous frameshift variant causes dilated cardiomyopathy and left ventricular noncompaction cardiomyopathy.
Guo J et al.
Molecular Genetics & Genomic Medicine, 2019
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