Nakamura, M., Sanuki, R., Yasuma, T., Onishi, A., Nishiguchi, K. M., Koike, C., . . . Furukawa, T. (2010). TRPM1 mutations are associated with the complete form of congenital stationary night blindness. Molecular Vision.
Citação norma ChicagoNakamura, Makoto, et al. TRPM1 Mutations Are Associated With the Complete Form of Congenital Stationary Night Blindness. Molecular Vision, 2010.
Citação norma MLANakamura, Makoto, et al. TRPM1 Mutations Are Associated With the Complete Form of Congenital Stationary Night Blindness. Molecular Vision, 2010.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.