A novel splicing mutation in the V2 vasopressin receptor. [electronic resource]
Producer: 20010301Description: 43-9 p. digitalISSN:- 0931-041X
- Alternative Splicing
- Amino Acid Sequence
- Amino Acid Substitution
- Base Sequence
- Child, Preschool
- Deamino Arginine Vasopressin
- Denmark
- Diabetes Insipidus, Nephrogenic -- diagnosis
- Female
- Genomic Imprinting
- Humans
- Male
- Molecular Sequence Data
- Pedigree
- Point Mutation
- Polymerase Chain Reaction
- Protein Structure, Secondary
- Receptors, Vasopressin -- chemistry
- X Chromosome
No physical items for this record
Publication Type: Case Reports; Journal Article
There are no comments on this title.
Log in to your account to post a comment.