Arikawa-Hirasawa, E., Le, A. H., Nishino, I., Nonaka, I., Ho, N. C., Francomano, C. A., . . . Yamada, Y. (2002). Structural and Functional Mutations of the Perlecan Gene Cause Schwartz-Jampel Syndrome, with Myotonic Myopathy and Chondrodysplasia. The American Society of Human Genetics.
Citação norma ChicagoArikawa-Hirasawa, Eri, et al. Structural and Functional Mutations of the Perlecan Gene Cause Schwartz-Jampel Syndrome, With Myotonic Myopathy and Chondrodysplasia. The American Society of Human Genetics, 2002.
Citação norma MLAArikawa-Hirasawa, Eri, et al. Structural and Functional Mutations of the Perlecan Gene Cause Schwartz-Jampel Syndrome, With Myotonic Myopathy and Chondrodysplasia. The American Society of Human Genetics, 2002.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.