Associated Papers
Exploring pathogenesis, prevalence, and genetic associations in Chiari malformation type 1: a contemporary perspective.
Mohd Rosdi SN et al.
Asian Biomedicine : Research, Reviews and News, 2024
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A8-A06P-01A.domain
Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation.
Doss S et al.
Journal of Neurology, 2014
Select a paper to view details