Monin, M., Mignot, C., De Lonlay, P., Héron, B., Masurel, A., Mathieu-Dramard, M., . . . Héron, D. (2014). 29 French adult patients with PMM2-congenital disorder of glycosylation: Outcome of the classical pediatric phenotype and depiction of a late-onset phenotype. BioMed Central.
Chicago Style CitationMonin, Marie-Lorraine, et al. 29 French Adult Patients With PMM2-congenital Disorder of Glycosylation: Outcome of the Classical Pediatric Phenotype and Depiction of a Late-onset Phenotype. BioMed Central, 2014.
MLA CitationMonin, Marie-Lorraine, et al. 29 French Adult Patients With PMM2-congenital Disorder of Glycosylation: Outcome of the Classical Pediatric Phenotype and Depiction of a Late-onset Phenotype. BioMed Central, 2014.
Warning: These citations may not always be 100% accurate.