Cite
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
MLA
Nazif Muhammad, et al. “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.” Frontiers in Neurology, vol. 14, May 2023. EBSCOhost, https://doi.org/10.3389/fneur.2023.1168307.
APA
Nazif Muhammad, Syeda Iqra Hussain, Zia Ur Rehman, Sher Alam Khan, Samin Jan, Niamatullah Khan, Muhammad Muzammal, Sumra Wajid Abbasi, Naseebullah Kakar, Muzammil Ahmad Khan, Muhammad Usman Mirza, Noor Muhammad, Saadullah Khan, & Naveed Wasif. (2023). 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. Frontiers in Neurology, 14. https://doi.org/10.3389/fneur.2023.1168307
Chicago
Nazif Muhammad, Syeda Iqra Hussain, Zia Ur Rehman, Sher Alam Khan, Samin Jan, Niamatullah Khan, Muhammad Muzammal, et al. 2023. “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.” Frontiers in Neurology 14 (May). doi:10.3389/fneur.2023.1168307.