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Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients.
- Source :
- Human Molecular Genetics; Apr2010, Vol. 19 Issue 8, p1399-1412, 14p
- Publication Year :
- 2010
Details
- Language :
- English
- ISSN :
- 09646906
- Volume :
- 19
- Issue :
- 8
- Database :
- Complementary Index
- Journal :
- Human Molecular Genetics
- Publication Type :
- Academic Journal
- Accession number :
- 48983312
- Full Text :
- https://doi.org/10.1093/hmg/ddq015