Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency. [electronic resource]
Producer: 19951102Description: 144-9 p. digitalISSN:- 1061-4036
- Amino Acid Sequence
- Animals
- Base Sequence
- Cattle
- Cell Nucleus -- enzymology
- Chromosome Mapping
- Chromosomes, Human, Pair 3
- Cloning, Molecular
- Consanguinity
- DNA Primers
- Electron Transport Complex II
- Electron Transport Complex IV -- metabolism
- Female
- Fibroblasts -- enzymology
- Homozygote
- Humans
- Lymphocytes -- enzymology
- Male
- Mitochondria -- enzymology
- Mitochondria, Muscle -- enzymology
- Molecular Sequence Data
- Multienzyme Complexes -- deficiency
- Muscle, Skeletal -- enzymology
- Mutagenesis, Site-Directed
- Nuclear Family
- Oxidoreductases -- deficiency
- Pedigree
- Point Mutation
- Restriction Mapping
- Saccharomyces cerevisiae -- enzymology
- Sequence Homology, Amino Acid
- Succinate Dehydrogenase -- biosynthesis
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.