Associated Papers
Simultaneous detection of small and large variants enhances the diagnosis of rare diseases using full genome sequencing.
Tsai MM et al.
Human Molecular Genetics, 2026
Synonymous and non-synonymous variants at splice junctions can disrupt splicing and are frequently linked to disease associated loss of function genes.
Srinivasan S et al.
Bmc Genomics, 2025
41436921 (PubMed )
Supplement: 12864_2025_12466_MOESM15_ESM.pdf
An X-Linked Ataxia Syndrome in a Family with Hearing Loss Associated with a Novel Variant in the BCAP31 Gene.
Paucar M et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2025
39831730 (PubMed )
Supplement: MDS-40-672-s006.pdf
Case Report: The first Korean familial case of BCAP31-related deafness, dystonia, and cerebral hypomyelination.
Suh YA et al.
Frontiers in Pediatrics, 2024
De novo mutation and skewed X-inactivation in girl with BCAP31-related syndrome.
Kao HJ et al.
Human Mutation, 2020
Select a paper to view details