Article
Update on genetic and molecular investigations of diseases with general impairment of peroxisomal functions.
Biochimie - 1 Jan 1993
Bioukar E B, Deschatrette J
Abstract excerpt
A group of genetically determined peroxisomal diseases is characterized by both multiple enzymatic deficiencies and abnormal structural features of the organelle. The primary cause of the phenotypes is likely to involve peroxisome assembly impairment. Complementation analyses performed on fibroblasts of patients revealed the existence of at least eight groups that do not reflect the clinical classifications....
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