Associated Papers
Unraveling the function and structure impact of deleterious missense SNPs in the human OX1R receptor by computational analysis.
Farajzadeh-Dehkordi M et al.
Scientific Reports, 2024
38191899 (PubMed )
Supplement: 41598_2023_49809_MOESM5_ESM.xlsx › Table_S2
Characterization of Disease-Associated Mutations in Human Transmembrane Proteins.
Molnár J et al.
Plos One, 2016
26986070 (PubMed )
Supplement: pone.0151760.s001.xlsx › polymorphism
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