Article Versions Notes

Ramzan S, Tennstedt S, Tariq M, Khan S, Noor Ul Ayan H, Ali A, Munz M, Thiele H, Korejo AA, Mughal AR, et al. A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family. Genes. 2021; 12(8):1282. https://doi.org/10.3390/genes12081282

Ramzan, Shafaq, Stephanie Tennstedt, Muhammad Tariq, Sheraz Khan, Hafiza Noor Ul Ayan, Aamir Ali, Matthias Munz, Holger Thiele, Asad Aslam Korejo, Abdul Razzaq Mughal, and et al. 2021. "A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family" Genes 12, no. 8: 1282. https://doi.org/10.3390/genes12081282

Ramzan, S., Tennstedt, S., Tariq, M., Khan, S., Noor Ul Ayan, H., Ali, A., Munz, M., Thiele, H., Korejo, A. A., Mughal, A. R., Jamal, S. Z., Nürnberg, P., Baig, S. M., Erdmann, J., & Ahmad, I. (2021). A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family. Genes, 12(8), 1282. https://doi.org/10.3390/genes12081282