Article
Allelic association and linkage studies in Wilson disease.
Human molecular genetics - 1 Sept 1993
Thomas G R, Roberts E A, Rosales T O, Moroz S P, Lambert M A, Wong L T, Cox D W
Abstract excerpt
We have studied 21 families with Wilson disease (WND), using restriction fragment length polymorphisms (RFLPs) in the 13q14.3 region, to measure linkage of these markers to the disease locus. In addition to previously described markers, we include linkage data for a newly isolated marker (D13S86)...
Topics
- Alleles
- Base Sequence
- Chromosome Mapping
- Chromosomes, Human, Pair 13
- DNA
- Female
- Genetic Linkage
- Genetic Markers
- Genotype
- Hepatolenticular Degeneration
- Humans
- Lod Score
- Male
- Molecular Sequence Data
- Pedigree
- Polymorphism, Restriction Fragment Length
