Raas-Rothschild, A., Wanders, R. J. A., Mooijer, P. A. W., Gootjes, J., Waterham, H. R., Gutman, A., . . . Korman, S. H. (2002). A PEX6-Defective Peroxisomal Biogenesis Disorder with Severe Phenotype in an Infant, versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents. The American Society of Human Genetics.
Chicago Style CitationRaas-Rothschild, Annick, et al. A PEX6-Defective Peroxisomal Biogenesis Disorder With Severe Phenotype in an Infant, Versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents. The American Society of Human Genetics, 2002.
Cita MLARaas-Rothschild, Annick, et al. A PEX6-Defective Peroxisomal Biogenesis Disorder With Severe Phenotype in an Infant, Versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents. The American Society of Human Genetics, 2002.