Peroxisome biogenesis disorders
National Institutes of Health
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The biogenesis of peroxisomal matrix and membrane proteins is substantially different from the biogenesis of proteins of other…
The peroxisome biogenesis disorders (PBDs) comprise 12 autosomal recessive complementation groups (CGs). The multisystem clinical…
Inherited aberrant peroxisome assembly results in a group of neurological diseases termed peroxisome biogenesis disorders (PBDs…
Human peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal-recessive diseases caused by…
The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous diseases lethal in early infancy1. Although…
In humans, defects in peroxisome assembly result in the peroxisome biogenesis disorders (PBDs), a group of genetically…
The peroxisome biogenesis disorders (PBDs) are lethal recessive diseases caused by defects in peroxisome assembly. We have…
The peroxisome is a ubiquitous, subcellular organelle containing more than 50 matrix enzymes that participate in a diverse array…