Associated Papers
Novel SCN9A variant associated with congenital insensitivity to pain.
Yammine T et al.
Molecular Biology Reports, 2023
Targeted next-generation sequencing as a comprehensive test for Mendelian diseases: a cohort diagnostic study.
Sun Y et al.
Scientific Reports, 2018
30076350 (PubMed )
Supplement: 41598_2018_30151_MOESM1_ESM.docx
Select a paper to view details