A new mutation within the porphobilinogen deaminase gene leading to a truncated protein as a cause of acute intermittent porphyria in an extended Indian family. [electronic resource]
Producer: 20080116Description: 194-201 p. digitalISSN:- 0015-5500
- Amino Acid Sequence
- Base Sequence
- DNA Mutational Analysis
- Electrophoresis, Polyacrylamide Gel
- Family
- Female
- Heme -- metabolism
- Humans
- Hydroxymethylbilane Synthase -- chemistry
- India
- Male
- Middle Aged
- Molecular Sequence Data
- Mutant Proteins -- metabolism
- Mutation -- genetics
- Pedigree
- Porphyria, Acute Intermittent -- enzymology
- Protein Structure, Secondary
- Recombinant Fusion Proteins
No physical items for this record
Publication Type: 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.