APA (7th ed.) Citation

Jadidi, M., Babaali, V., InanlooRahatloo, K., Salehi, N., & Mollazadeh, R. Identification of a rare variant in TNNT3 responsible for familial dilated cardiomyopathy through whole-exome sequencing and in silico analysis. BMC.

Chicago Style (17th ed.) Citation

Jadidi, Motahareh, Vida Babaali, Kolsoum InanlooRahatloo, Najmeh Salehi, and Reza Mollazadeh. Identification of a Rare Variant in TNNT3 Responsible for Familial Dilated Cardiomyopathy Through Whole-exome Sequencing and in Silico Analysis. BMC.

MLA (9th ed.) Citation

Jadidi, Motahareh, et al. Identification of a Rare Variant in TNNT3 Responsible for Familial Dilated Cardiomyopathy Through Whole-exome Sequencing and in Silico Analysis. BMC.