Nazif Muhammad
Kohat, KP, Pakistan
Last Updated: 09/26/2026
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Found 10 publications
The Genetic Basis of Neurological Disorders: Missense and Nonsense Variants in Three Pakistani Families With Syndromic Intellectual Disability.
Journal: Annals of human genetics
Published: August 28, 2025
Truncated Variants in FAM20A and WDR72 Genes Underlie Autosomal Recessive Amelogenesis Imperfecta in Four Pakistani Families.
Journal: Biochemical genetics
Published: January 13, 2025
Variants in HCFC1 and MN1 genes causing intellectual disability in two Pakistani families.
Journal: BMC medical genomics
Published: March 25, 2024
Molecular insight into CREBBP and TANGO2 variants causing intellectual disability.
Journal: The journal of gene medicine
Published: July 11, 2023
Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability.
Journal: BMC neurology
Published: May 24, 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.
Journal: Frontiers in neurology
Published: February 17, 2023
Biallelic mutations in FLG, TGM1, and STS genes segregated with different types of ichthyoses in eight families of Pakistani origin.
Journal: International journal of dermatology
Published: September 26, 2022
Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function.
Journal: Human mutation
Published: May 03, 2022
A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family.
Journal: BMC medical genetics
Published: October 14, 2019
Showing 1-10 of 10
Last Updated: 09/26/2026