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Soumeya Bekri
Department of Biochemistry
Centre Hospitalier Universitaire de Nice
France
Name/email consistency: high
- Fabry disease in patients with end-stage renal failure: the potential benefits of screening. Bekri, S., Enica, A., Ghafari, T., Plaza, G., Champenois, I., Choukroun, G., Unwin, R., Jaeger, P. Nephron. Clin. Pract (2005)
- Early diagnosis of mucopolysaccharidosis III A with a nonsense mutation and two de novo missense mutations in SGSH gene. Bekri, S., Armana, G., De Ricaud, D., Osenda, M., Maire, I., Van Obberghen, E., Froissart, R. J. Inherit. Metab. Dis. (2005)
- The molecular basis of succinic semialdehyde dehydrogenase deficiency in one family. Bekri, S., Fossoud, C., Plaza, G., Guenne, A., Salomons, G.S., Jakobs, C., Van Obberghen, E. Mol. Genet. Metab. (2004)
