Article
Peroxisome biogenesis disorders.
Annual review of genomics and human genetics - 1 Jan 2003
Weller Sabine, Gould Stephen J, Valle David
Abstract excerpt
The peroxisome biogenesis disorders (PBDs) comprise 12 autosomal recessive complementation groups (CGs). The multisystem clinical phenotype varies widely in severity and results from disturbances in both development and metabolic homeostasis. Progress over the last several years has lead to identification of the genes responsible for all of these disorders and to a much improved understanding of the biogenesis...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.