Bespalova, I. Et Al. 2001. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.. AMERICAN JOURNAL OF HUMAN GENETICS , vol.69, no.4 , 230.

Bespalova, I., Van Camp, G., Bom, S., Brown, D., Cryns, K., DeWan, A., ... Erson, A. E.(2001). Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.. AMERICAN JOURNAL OF HUMAN GENETICS , vol.69, no.4, 230.

Bespalova, IN Et Al. "Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.," AMERICAN JOURNAL OF HUMAN GENETICS , vol.69, no.4, 230, 2001

Bespalova, IN Et Al. "Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.." AMERICAN JOURNAL OF HUMAN GENETICS , vol.69, no.4, pp.230, 2001

Bespalova, I. Et Al. (2001) . "Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.." AMERICAN JOURNAL OF HUMAN GENETICS , vol.69, no.4, p.230.

@article{article, author={IN Bespalova Et Al. }, title={Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2001, pages={230} }