Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase gene. [electronic resource]
Producer: 19970715Description: 563-9 p. digitalISSN:- 0964-6906
- Chromosome Mapping
- Chromosomes, Human, Pair 19 -- genetics
- Creatine Kinase -- genetics
- DNA Primers
- Female
- Genetic Markers
- Genetic Testing
- Genotype
- Glutarates -- urine
- Humans
- Iraq
- Isoenzymes
- Jews
- Linkage Disequilibrium -- genetics
- Lod Score
- Male
- Myotonin-Protein Kinase
- Optic Atrophy -- genetics
- Pedigree
- Polymorphism, Genetic -- genetics
- Protein Serine-Threonine Kinases -- chemistry
- Trinucleotide Repeats -- genetics
No physical items for this record
Publication Type: Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
There are no comments on this title.
Log in to your account to post a comment.