Article
The molecular biology of human hereditary central diabetes insipidus.
Progress in brain research - 1 Jan 1992
Repaske D R, Phillips J A
Abstract excerpt
Molecular biology techniques have begun to shed light on the genetic basis of autosomal dominant central DI, but several very basic questions remain to be answered. The disorder was initially presumed to have a developmental, degenerative, or autoimmune basis based on the autopsy findings in the...
Topics
- Animals
- Arginine Vasopressin
- Deoxyribonuclease HpaII
- Deoxyribonucleases, Type II Site-Specific
- Diabetes Insipidus
- Female
- Genetic Linkage
- Haplotypes
- Humans
- Male
- Molecular Biology
- Mutation
- Pedigree
- Polymorphism, Restriction Fragment Length
- Rats
