BESPALOVA, I. Et Al. 2001. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss. HUMAN MOLECULAR GENETICS , vol.10, no.22 , 2501-2508.

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. HUMAN MOLECULAR GENETICS , vol.10, no.22, 2501-2508.

BESPALOVA, IN Et Al. "Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss," HUMAN MOLECULAR GENETICS , vol.10, no.22, 2501-2508, 2001

BESPALOVA, IN Et Al. "Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss." HUMAN MOLECULAR GENETICS , vol.10, no.22, pp.2501-2508, 2001

BESPALOVA, I. Et Al. (2001) . "Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss." HUMAN MOLECULAR GENETICS , vol.10, no.22, pp.2501-2508.

@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={HUMAN MOLECULAR GENETICS}, year=2001, pages={2501-2508} }