Human genetic diseases due to codon reiteration: Relationship to an evolutionary mechanism
- 1 September 1993
- Vol. 74 (6) , 955-956
- https://doi.org/10.1016/0092-8674(93)90718-6
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomesCell, 1993
- Triplet repeat mutations in human diseaseScience, 1992
- An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular DystrophyScience, 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
- Transglutaminases: multifunctional cross‐linking enzymes that stabilize tissuesThe FASEB Journal, 1991
- Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophyNature, 1991
- Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) nScience, 1991
- The Human Androgen Receptor: Complementary Deoxyribonucleic Acid Cloning, Sequence Analysis and Gene Expression in ProstateMolecular Endocrinology, 1988
- Structure and evolution of the human involucrin geneCell, 1986
- TransglutaminasesMolecular and Cellular Biochemistry, 1984