Torkamandi, S., Rezaei, S., Mirfakhraie, R., Bayat, S., Piltan, S., & Gholami, M. (2020). A homozygous missense mutation of WFS1 gene causes Wolfram's syndrome without hearing loss in an Iranian family (a report of clinical heterogeneity). J Clin Lab Anal.

Torkamandi, Shahram, Somaye Rezaei, Reza Mirfakhraie, Sahar Bayat, Samira Piltan, and Milad Gholami. "A Homozygous Missense Mutation of WFS1 Gene Causes Wolfram's Syndrome Without Hearing Loss in an Iranian Family (a Report of Clinical Heterogeneity)." J Clin Lab Anal 2020.

Torkamandi, Shahram, et al. "A Homozygous Missense Mutation of WFS1 Gene Causes Wolfram's Syndrome Without Hearing Loss in an Iranian Family (a Report of Clinical Heterogeneity)." J Clin Lab Anal 2020.