Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillation

por Malakootian, Mahshid, Jalilian, Masoumeh, Kalayinia, Samira, Hosseini Moghadam, Maryam, Heidarali, Mona, Haghjoo, Majid
Publicado 2022

Endothelial nitric oxide synthase Asp298Glu (894G/T) gene polymorphism as a possible risk factor for the coronary slow flow phenomenon among Iranians

por Karimi, Yeganeh, Sehati, Fatemeh, Sarreshtedari, Ali, Mirzad, Mina, Khalili, Yasaman, Kiani, Reza, Taheri Bajgan, Elham, Hosseini Moghadam, Maryam, Mehrvarz, Farzaneh, Bakhshandeh, Hooman, Parham, Maryam, Malakootian, Mahshid, Sadeghipour, Parham
Publicado 2022