Muhammad Ayub
Quetta, BA, Pakistan
Last Updated: 09/26/2026
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Found 9 publications
Author Correction: Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.
Journal: Nature genetics
Published: August 26, 2025
Highly sensitive electrochemical detection and quantification of opium derived morphine sulfate using cysteamine loaded MWCNTs@V2O5 telluride composite.
Journal: Scientific reports
Published: May 24, 2025
A TMC8 splice variant causes epidermodysplasia verruciformis in a Pakistani family.
Journal: Clinical and experimental dermatology
Published: October 21, 2022
Identification and In Silico Analysis of a Homozygous Nonsense Variant in TGM1 Gene Segregating with Congenital Ichthyosis in a Consanguineous Family.
Journal: Medicina (Kaunas, Lithuania)
Published: October 18, 2022
Novel Frameshift Mutations in XPC Gene Underlie Xeroderma Pigmentosum in Pakistani Families.
Journal: Indian journal of dermatology
Published: June 30, 2021
Genetics Of Human Hereditary Hearing Impairment.
Journal: Journal of Ayub Medical College, Abbottabad : JAMC
Published: January 14, 2018
Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosis.
Journal: International journal of dermatology
Published: September 02, 2014
Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86.
Journal: American journal of human genetics
Published: October 31, 2013
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Last Updated: 09/26/2026