Tam H. Nguyen

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

G. Kay, D. Crane, C. Paterson, 2003, Molecular and Cellular Biology.

Quantitative genotyping of mouse brain-specific PEX13 gene disruption by real-time PCR

D. Crane, J. Nourse, Tam H. Nguyen, 2009, Journal of Neuroscience Methods.

PEX13 deficiency in mouse brain as a model of Zellweger syndrome: abnormal cerebellum formation, reactive gliosis and oxidative stress

D. Crane, B. Ahlemeyer, E. Baumgart-Vogt, 2010, Disease Models & Mechanisms.

PEX13 deficiency in mouse brain as a model of Zellweger syndrome: abnormal cerebellum formation, reactive gliosis and oxidative stress

D. Crane, B. Ahlemeyer, Sharp, 2010, Disease Models & Mechanisms.

Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundance

D. Crane, Tam Nguyen, Jonas Bjorkman, 2006, Journal of Cell Science.

Deletion Syndrome

A. L. Wong, F. Mastaglia, M. Benatar, 2019 .

PEX13 deficiency in mouse brain as a model of Zellweger syndrome: abnormal cerebellum formation, reactive gliosis and oxidative stress

D. Crane, B. Ahlemeyer, E. Baumgart-Vogt, 2010, Disease Models & Mechanisms.