Associated Papers
A novel non-sense variant in GSDME causing exon skipping associated with DFNA5 in a large Chinese family.
Yang B et al.
Frontiers in Neurology, 2026
41725728 (PubMed )
Supplement: Table_1.xlsx › Variants_in_IV-4
Potential susceptibility genes in patients with stage III and IV periodontitis: A whole-exome sequencing pilot study.
Xue F et al.
Biomolecules & Biomedicine, 2024
Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes.
Guo H et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
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