Identification of two variant short chain acyl-coenzyme A dehydrogenase alleles, each containing a different point mutation in a patient with short chain acyl-coenzyme A dehydrogenase deficiency. [electronic resource]
Producer: 19900606Description: 1575-82 p. digitalISSN:- 0021-9738
- Acyl-CoA Dehydrogenases -- deficiency
- Alleles
- Blotting, Southern
- Butyryl-CoA Dehydrogenase
- Cell Line
- Cells, Cultured
- Cloning, Molecular
- Female
- Genetic Variation
- Genomic Library
- Humans
- Lipid Metabolism, Inborn Errors -- enzymology
- Mutation
- Polymerase Chain Reaction
- RNA -- genetics
- RNA, Messenger -- genetics
- Reference Values
- Restriction Mapping
No physical items for this record
Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
There are no comments on this title.
Log in to your account to post a comment.