एपीए उद्धरण

Khan, M. I., Collin, R. W., Arimadyo, K., Micheal, S., Azam, M., Qureshi, N., . . . Cremers, F. P. (2010). Missense mutations at homologous positions in the fourth and fifth laminin A G-like domains of eyes shut homolog cause autosomal recessive retinitis pigmentosa. Molecular Vision.

शिकागो स्टाइल उद्धरण

Khan, Muhammad Imran, et al. Missense Mutations At Homologous Positions in the Fourth and Fifth Laminin A G-like Domains of Eyes Shut Homolog Cause Autosomal Recessive Retinitis Pigmentosa. Molecular Vision, 2010.

एमएलए उद्धरण

Khan, Muhammad Imran, et al. Missense Mutations At Homologous Positions in the Fourth and Fifth Laminin A G-like Domains of Eyes Shut Homolog Cause Autosomal Recessive Retinitis Pigmentosa. Molecular Vision, 2010.

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