Hafiza Noor Ul Ayan
2PUBLICATIONS
7CO-AUTHORS
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Publications (2)
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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
|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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