Associated Papers
ClinGen Variant Curation Interface Workshops: Training Variant Scientists on an International Platform.
Ritter DI et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
Reanalysis of Exome Sequencing Data in the Indian Undiagnosed Diseases Program: Improving Diagnostic Yield and Ending Diagnostic Odyssey.
Garg N et al.
Clinical Genetics, 2025
A novel homozygous synonymous splicing variant in SELENOI gene causes spastic paraplegia 81.
Sarma AS et al.
The Journal of Gene Medicine, 2023
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