Muzammil Ahmad Khan
8PUBLICATIONS
10CO-AUTHORS
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Publications (8)
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|Feb 13, 2026
A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani family.Sana Fatima, Dong Sun, Jianguo Han
|Apr 28, 2023
Identification of GLI1 and KIAA0825 Variants in Two Families with Postaxial Polydactyly.Safeer Ahmad, Muhammad Zeeshan Ali, Muhammad Muzammal
|Jul 30, 2022
The molecular genetics of human appendicular skeleton.Safeer Ahmad, Muhammad Zeeshan Ali, Muhammad Muzammal
|Apr 23, 2022
In Silico Analysis of the L-2-Hydroxyglutarate Dehydrogenase Gene Mutations and Their Biological Impact on Disease Etiology.Muhammad Muzammal, Alessandro Di Cerbo, Eman M Almusalami
|Apr 23, 2022
In Silico Analysis Identified Putative Pathogenic Missense nsSNPs in Human SLITRK1 Gene.Muhammad Zeeshan Ali, Arshad Farid, Safeer Ahmad
|Jan 11, 2020
Identification of a novel protein truncating mutation p.Asp98* in XPC associated with xeroderma pigmentosum in a consanguineous Pakistani family.Muhammad Z Ali, Jasmin Blatterer, Muzammil A Khan
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Frequent Collaborators
2 joint publications
Arshad Farid
2 joint publications
Mohammed Al Mohaini
2 joint publications
Maitham A Al Hawaj
2 joint publications
Yousef N Alhashem
1 joint publications
Ejazullah Khan
1 joint publications
Saadullah Khan
1 joint publications
Alessandro Di Cerbo
1 joint publications
Abdulmonem A Alsaleh
1 joint publications
Outi Mäkitie
1 joint publications
Muhammad Muzammal
