Associated Papers
Novel mutation SLFN14 T853fs associated with inherited macrothrombocytopenia.
Xie H et al.
Molecular Therapy. Nucleic Acids, 2025
Severe Thrombocytopenia Is Associated with a Genetic Variant in the Helicase Domain of SLFN14 Gene: A Case Report.
Yang K et al.
Ejhaem, 2025
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
Identification of Two Mutations in PCDHGA4 and SLFN14 Genes in an Atrial Septal Defect Family.
Su W et al.
Current Medical Science, 2018
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