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.
Okumoto, K
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] - Molecular and cellular biology Jul 1998 - 4324-36 p. digital
Publication Type: Journal Article
0270-7306
10.1128/MCB.18.7.4324 doi
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
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] - Molecular and cellular biology Jul 1998 - 4324-36 p. digital
Publication Type: Journal Article
0270-7306
10.1128/MCB.18.7.4324 doi
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