Mutations participating in interallelic complementation in propionic acidemia. [electronic resource]
Producer: 19940729Description: 51-8 p. digitalISSN:- 0002-9297
- Alleles
- Amino Acid Metabolism, Inborn Errors -- genetics
- Amino Acid Sequence
- Base Sequence
- Binding Sites
- Carboxy-Lyases -- chemistry
- Cell Line
- Conserved Sequence
- DNA Mutational Analysis
- Frameshift Mutation
- Genetic Complementation Test
- Humans
- Methylmalonyl-CoA Decarboxylase
- Molecular Sequence Data
- Mutagenesis, Insertional
- Mutation
- Point Mutation
- Propionates -- blood
- Propionibacterium -- genetics
- Sequence Deletion
- Sequence Homology, Amino Acid
- Suppression, Genetic
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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