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Amirian, A. and Zafari, Z. and Karimipoor, M. and Kordafshari, A. and Dalili, M. and Saber, S. and Fazelifar, A.F. and Zeinali, S. (2019) Identification of a novel KCNQ1 frameshift mutation and review of the literature among iranian long QT families. Iranian Biomedical Journal, 23 (3). pp. 228-234.
Amirian, A. and Zafari, Z. and Dalili, M. and Saber, S. and Karimipoor, M. and Dabbagh Bagheri, S. and Fazelifar, A.F. and Zeinali, S. (2018) Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange-Nielsen syndrome in 2 Iranian families. Journal of Arrhythmia.
Amirian, A. and Zafari, Z. and Dalili, M. and Saber, S. and Karimipoor, M. and Bagheri, S.D. and Fazelifar, A.F. and Zeinali, S. (2018) Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange-Nielsen syndrome in 2 Iranian families. Journal of Arrhythmia, 34 (3). pp. 286-290.
Amirian, A. and Zafari, Z. and Dalili, M. and Saber, S. and Karimipoor, M. and Dabbagh Bagheri, S. and Fazelifar, A.F. and Zeinali, S. (2018) Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange-Nielsen syndrome in 2 Iranian families. Journal of Arrhythmia.
Amirian, A. and Dalili, S.M. and Zafari, Z. and Saber, S. and Karimipoor, M. and Akbari, V. and Fazelifar, A.F. and Zeinali, S. (2018) Novel frameshift mutation in the KCNQ1 gene responsible for jervell and lange-nielsen syndrome. Iranian Journal of Basic Medical Sciences, 21 (1). pp. 108-111.
Amirian, A. and Dalili, S.M. and Zafari, Z. and Saber, S. and Karimipoor, M. and Akbari, V. and Fazelifar, A.F. and Zeinali, S. (2018) Novel frameshift mutation in the KCNQ1 gene responsible for jervell and lange-nielsen syndrome. Iranian Journal of Basic Medical Sciences, 21 (1). pp. 108-111.
