एपीए उद्धरण

Ahmed, Z. M., Masmoudi, S., Kalay, E., Belyantseva, I. A., Mosrati, M. A., Collin, R. W. J., . . . Kremer, H. (2008). Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.

शिकागो स्टाइल उद्धरण

Ahmed, Zubair M., et al. Mutations of LRTOMT, a Fusion Gene With Alternative Reading Frames, Cause Nonsyndromic Deafness in Humans. 2008.

एमएलए उद्धरण

Ahmed, Zubair M., et al. Mutations of LRTOMT, a Fusion Gene With Alternative Reading Frames, Cause Nonsyndromic Deafness in Humans. 2008.