Sharp, Peter

Pex13 Inactivation in the Mouse Disrupts Peroxisome Biogenesis and Leads to a Zellweger Syndrome Phenotype

Maxwell, M., Bjorkman, J., Nguyen, T., Sharp, P., Finnie, J., Paterson, C., Tonks, I., Paton, B. C., Kay, G. F., & Crane, D. I. (2003) · Molecular and Cellular Biology

Metabolism and Genetic DisordersGlycogen Storage Diseases and Myoclonus

Cited by 110

Pitfalls in the prenatal diagnosis of peroxisomal β‐oxidation defects by chorionic villus sampling

Carey, W. F., Poulos, A., Sharp, P., Nelson, P. V., Robertson, E. F., Hughes, J. L., & Gill, A. (1994) · Prenatal Diagnosis

Metabolism and Genetic DisordersPrenatal Screening and Diagnostics

Cited by 22