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