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.

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