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BMC Medical Genomics|July 3, 2024
Variants in HCFC1 and MN1 genes causing intellectual disability in two Pakistani familiesSyeda Iqra Hussain, Nazif Muhammad, Shahbaz Ali Shah, et al.The Journal of Gene Medicine|September 18, 2023
Molecular insight into CREBBP and TANGO2 variants causing intellectual disabilitySyeda Iqra Hussain, Nazif Muhammad, Niamatullah Khan, et al.Annals of Human Genetics|December 5, 2025
The Genetic Basis of Neurological Disorders: Missense and Nonsense Variants in Three Pakistani Families With Syndromic Intellectual DisabilityKenza Javed, Nazif Muhammad, Syeda Iqra Hussain, et al.Frontiers in Neurology|June 12, 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 mechanismsNazif Muhammad, Syeda Iqra Hussain, Zia Ur Rehman, et al.BMC Neurology|October 4, 2023
Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disabilitySyeda Iqra Hussain, Nazif Muhammad, Salah Ud Din Shah, et al.Human Mutation|April 14, 2025
Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3)Seda Susgun, Afif Ben-Mahmoud, Franz Rüschendorf, et al.Pageof 1