Ilyas Ahmad

5PUBLICATIONS
14CO-AUTHORS
Respiratory diseasesGene and molecular therapyHaematologyNeurology and neuromuscular diseasesCardiology (incl. cardiovascular diseases)
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Publications (5)

|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

|Oct 10, 2022
A novel MAP3K20 mutation causing centronuclear myopathy-6 with fiber-type disproportion in a Pakistani family.

Ilyas Ahmad, Ayaz Khan, Hafiza Noor Ul Ayan

|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