Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation. [electronic resource]
Producer: 20030924Description: 233-46 p. digitalISSN:- 0002-9297
- Amino Acid Sequence
- Animals
- CHO Cells
- Catalase -- metabolism
- Cell Line
- Cricetinae
- DNA -- genetics
- DNA Mutational Analysis
- Female
- Gene Expression
- Genetic Complementation Test
- Genotype
- Humans
- Membrane Proteins -- deficiency
- Mice
- Molecular Sequence Data
- Mutation
- Peroxisomal Disorders -- classification
- Peroxisome-Targeting Signal 1 Receptor
- Phenotype
- Pregnancy
- RNA, Messenger -- genetics
- Receptors, Cytoplasmic and Nuclear -- metabolism
- Sequence Homology, Amino Acid
- Temperature
- Tissue Distribution
- Transfection
- Zellweger Syndrome -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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