Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders. [electronic resource]
Producer: 19981223Description: 1294-306 p. digitalISSN:- 0002-9297
- Amino Acid Sequence
- Base Sequence
- Cell Line
- Cells, Cultured
- Fibroblasts -- metabolism
- Genetic Complementation Test
- Genotype
- Humans
- Introns
- Membrane Proteins -- biosynthesis
- Molecular Sequence Data
- Oligodeoxyribonucleotides
- Open Reading Frames
- Peroxisomal Disorders -- genetics
- Phenotype
- Point Mutation
- Polymerase Chain Reaction
- Random Amplified Polymorphic DNA Technique
- Recombinant Proteins -- biosynthesis
- Transfection
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Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
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