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.
Citação norma ChicagoKhan, 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.
Citação norma MLAKhan, 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.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.