Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms

por Muhammad, Nazif, Hussain, Syeda Iqra, Rehman, Zia Ur, Khan, Sher Alam, Jan, Samin, Khan, Niamatullah, Muzammal, Muhammad, Abbasi, Sumra Wajid, Kakar, Naseebullah, Rehman, Zia Ur, Khan, Muzammil Ahmad, Mirza, Muhammad Usman, Muhammad, Noor, Khan, Saadullah, Wasif, Naveed
Publicado 2023

Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability

por Hussain, Syeda Iqra, Muhammad, Nazif, Shah, Salah Ud Din, Fardous, Fardous, Khan, Sher Alam, Khan, Niamatullah, Rehman, Adil U, Siddique, Mehwish, Wasan, Shoukat Ali, Niaz, Rooh, Ullah, Hafiz, Khan, Niamat, Muhammad, Noor, Mirza, Muhammad Usman, Wasif, Naveed, Khan, Saadullah
Publicado 2023