Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4
β Scribed by Polymeropoulos, Mihael H.; Swift, Ronnie Gorman; Swift, Michael
- Book ID
- 109917904
- Publisher
- Nature Publishing Group
- Year
- 1994
- Tongue
- English
- Weight
- 250 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1061-4036
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Aspartylglucosaminuria (AGU) is caused by deficient activity of the enzyme aspartylglucosaminidase (AGA). The structural gene for AGA has been assigned to the region 4q21-qter of chromosome 4. We have studied the map position of the AGU locus in relation to other marker loci on the long arm of chrom
The long QT syndrome is an autosomally dominantly inherited cardiac disorder characterized by abnormalities of myocardial repolarization, exercise-or stressrelated syncopal attacks and risk of sudden death due to cardiac arrhythmias. Genetic linkage studies have defined three LQT loci on chromosomes