PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p. [electronic resource]
Producer: 19980716Description: 4324-36 p. digitalISSN:- 0270-7306
- Amino Acid Sequence
- Animals
- Base Sequence
- CHO Cells
- Cell Line
- Cell Line, Transformed
- Cloning, Molecular
- Cricetinae
- Cytosol
- DNA, Complementary
- Fibroblasts
- Humans
- Membrane Proteins -- genetics
- Microbodies -- metabolism
- Molecular Sequence Data
- Mutagenesis
- Mutation
- Peroxisomal Disorders -- veterinary
- Rats
- Sequence Homology, Amino Acid
- Zellweger Syndrome -- genetics
- Zinc Fingers
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Publication Type: Journal Article
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