Triplet repeat disease is a group of hereditary neurodegenerative disorders caused by expansion of trinucleotide repeats such as CAG/CTG, CGG/CCG, and GAA/TTC. Direct detection of the expansion in the patient's genome shortcuts the tedious process needed for identification of disease genes by conven
Detection of the heteromorphic spectrum of heterochromatin in the human genome by in situ digestion using restriction endonucleaseAlui
β Scribed by Luke, Sunny ;Verma, Ram S.
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 439 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0148-7299
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