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.
Chicago Style aipamenaKhan, 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.
MLA aipamenaKhan, 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.
Kontuz: berrikusi erreferentzia hauek erabili aurretik.