Protein structural insights into a rare PCSK9 gain-of-function variant (R496W) causing familial hypercholesterolemia in a Saudi family: whole exome sequencing and computational ana...

por Shaik, Noor Ahmad, Al-Shehri, Najla, Athar, Mohammad, Awan, Ahmed, Khalili, Mariam, Al Mahadi, Hadiah Bassam, Hejazy, Gehan, Saadah, Omar I., Al-Harthi, Sameer Eida, Elango, Ramu, Banaganapalli, Babajan, Alefishat, Eman, Awan, Zuhier
Publicado 2023