https://www.selleckchem.com/products/q-vd-oph.html
Genetic analysis revealed segregation of several novel variants associated with HL, including a canonical splice-site variant (c.55-2AG) of PTPRQ in family GCFHL-01, a missense variant [c.1079GA; p.(Arg360Gln)] of SERPINB6 in family LUHL-01, and an insertion variant (c.10208-10211insCCACCAGGCCCGTGCCTC) within MYO15A in family LUHL-011. All the identified variants had very low frequencies in the control databases. The molecular modeling of p.Arg360Gln missense variant also predicted impaired folding of SERPINB6 protein. This stu
Like
Comment
Share
