Peroxisome biogenesis disorders
National Institutes of Health
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The application of current channelrhodopsin-based optogenetic tools is limited by the lack of strict ion selectivity and the…
Background: Peroxisome biogenesis disorders (PBDs) may have variable clinical expression, from severe, lethal to mild phenotypes…
Zellweger Syndrome is a rare autosomal recessive inherited disorder within the spectrum of peroxisome biogenesis disorders. It is…
L-Pipecolic acid oxidase activity is deficient in patients with peroxisome biogenesis disorders (PBDs). Because its role, if any…
Roundtable Discussion of Session 4: The Roles of DHA in Zellweger Syndrome, A Representative Peroxisomal Biogenesis Disorder…
To the Editor: Peroxisome biogenesis disorders (PBD) are fatal autosomal recessive diseases characterized by severe brain and…