Ilyas Ahmad
5PUBLICATIONS
14CO-AUTHORS
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Publications (5)
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|Feb 27, 2023
Homozygous frameshift variant in desmoglein 2 gene causes biventricular arrhythmogenic right ventricular cardiomyopathy.Hafiza Noor Ul Ayan, Pir Sheeraz Ali, Asad Aslam Korejo
|Feb 25, 2023
Novel Variants in MPV17, PRX, GJB1, and SACS Cause Charcot-Marie-Tooth and Spastic Ataxia of Charlevoix-Saguenay Type Diseases.Qaiser Zaman, Muhammad Abbas Khan, Kalsoom Sahar
|Jan 21, 2023
Report of Hermansky-Pudlak Syndrome in Two Families with Novel Variants in HPS3 and HPS4 Genes.Qaiser Zaman, Sadeeda, Muhammad Anas
|Aug 27, 2021
A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family.Shafaq Ramzan, Stephanie Tennstedt, Muhammad Tariq
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Frequent Collaborators
3 joint publications
Muhmmad Tariq
2 joint publications
Hafiza Noor Ul Ayan
2 joint publications
Peter Nürnberg
2 joint publications
Jeanette Erdmann
2 joint publications
Qaiser Zaman
2 joint publications
Gauhar Rehman
2 joint publications
Osama Yousef Muthaffar
2 joint publications
Musharraf Jelani
1 joint publications
Sheraz Khan
1 joint publications
Aamir Ali
