The Myotonic Dystrophy Gene
- 1 November 1993
- journal article
- review article
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 50 (11) , 1173-1179
- https://doi.org/10.1001/archneur.1993.00540110053005
Abstract
The myotonic dystrophy gene codes for a protein kinase and contains a repeated trinucleotide motif (adenine-guanine-cytosine [AGC]) in its transcribed sequence. The repeat is polymorphic in the general population, varying in size from five to 37 AGC units in normal alleles. Myotonic dystrophy patients show expansions of the repeated sequence from over 50 elements up to several thousand units. There is a positive correlation between repeat size and clinical severity. The direct analysis of the AGC repeat size allows an easy confirmation of the clinical diagnosis of myotonic dystrophy in difficult cases and for prenatal counseling.Keywords
This publication has 8 references indexed in Scilit:
- Different sex-dependent constraints in CTG length variation as explanation for congenital myotonic dystrophyThe Lancet, 1993
- Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophyNature Genetics, 1992
- Triplet repeat mutations in human diseaseScience, 1992
- Hypervariability of simple sequences as a general source for polymorphic DNA markersNucleic Acids Research, 1989
- ANTICIPATION IN MYOTONIC DYSTROPHY: FACT OR FICTION?Brain, 1989
- Characterization and expression of a cDNA encoding the human androgen receptor.Proceedings of the National Academy of Sciences, 1989
- ESTIMATION OF LINKAGE BETWEEN THE LUTHERAN AND THE LEWIS BLOOD GROUPSActa Pathologica Microbiologica Scandinavica, 1951
- THE PROBLEM OF ANTICIPATION IN PEDIGREES OF DYSTROPHIA MYOTONICAAnnals of Eugenics, 1947