Different sex-dependent constraints in CTG length variation as explanation for congenital myotonic dystrophy
- 23 January 1993
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 341 (8839) , 237
- https://doi.org/10.1016/0140-6736(93)90097-z
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophyNature Genetics, 1992
- An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular DystrophyScience, 1992
- Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the GeneScience, 1992
- Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family memberPublished by Elsevier ,1992
- Cloning of the essential myotonic dystrophy region and mapping of the putative defectNature, 1992
- Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophyNature, 1992
- Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophyNature, 1992