AHMED, Z. M. Et Al. 2008. Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans. NATURE GENETICS , vol.40, no.11 , 1335-1340.

AHMED, Z. M., MASMOUDI, S., Kalay, E., BELYANTSEVA, I. A., MOSRATI, M. A., COLLIN, R. W. J., ... RIAZUDDIN, S.(2008). Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans. NATURE GENETICS , vol.40, no.11, 1335-1340.

AHMED, Zubair Et Al. "Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans," NATURE GENETICS , vol.40, no.11, 1335-1340, 2008

AHMED, Zubair M. Et Al. "Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans." NATURE GENETICS , vol.40, no.11, pp.1335-1340, 2008

AHMED, Z. M. Et Al. (2008) . "Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans." NATURE GENETICS , vol.40, no.11, pp.1335-1340.

@article{article, author={Zubair M. AHMED Et Al. }, title={Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans}, journal={NATURE GENETICS}, year=2008, pages={1335-1340} }